Oh no. It looks like some Unilever has recalled some of their Skippy Peanut butter due to contamination with Salmonella.
The product was distributed to stores in Arkansas, Connecticut, Delaware, Illinois, Iowa, Maine, Minnesota, Missouri, Nebraska, New Hampshire, New Jersey, New York, North Dakota, Pennsylvania, Virginia and Wisconsin.
Some of the UPC producs affected by this recall are....(The UPCs codes are located on the side of the jar's label, below the bar code).
048001006812
048001006782
The will have the following Best if Used By Dates stamped on the lid of the jar:
MAY1612LR1
MAY1712LR1
MAY1812LR1
MAY1912LR1
MAY2012LR1
MAY2112LR1
Make sure you go on over here and check out the info that they have posted.
Thanks so much Living Rich with Coupons for the heads up on this!
Cheryl
Showing posts with label Recall. Show all posts
Showing posts with label Recall. Show all posts
Monday, March 7, 2011
Tuesday, October 26, 2010
**Recall** Nestle Raisinets
Nestle USA has just issued a voluntary recall on Rasinets Fun Size Bags because the candy MAY CONTAIN PEANUTS, which can cause potentially life-threatening reaction in people with allergies to peanuts (the peanuts were not included on the list of ingredients).
These Fun Size Bags (10 oz) have the production code of....02015748/UPC number 2800010255.
These bags were distrubuted ONLY in the U.S. to Target, Shop Rite, and Don Quixote retail stores.
The only product involved is Nestle Raisinets Fun Size Bags (10oz) distributed in the U.S. with a production code of 02015748/UPC number 2800010255. No other Nestlé products are impacted.
Nestle asked consumers to contact Nestle Consumer Services directly at 1-800-478-5670 for a full refund and discard any remaining packages. Consumers should NOT return Nestle Raisinets Fun Size Bags (10oz) with a production code of 02015748/UPC number 2800010255 to retailers. Operators are available between 8 a.m. and 8 p.m. EST and after hours for emergencies. Those with questions should contact Nestle Consumer Services at 1-800-478-5670 or via email at mailto:www.nestlecandy@casupport.com.
Thanks!
Cheryl
These Fun Size Bags (10 oz) have the production code of....02015748/UPC number 2800010255.
These bags were distrubuted ONLY in the U.S. to Target, Shop Rite, and Don Quixote retail stores.
The only product involved is Nestle Raisinets Fun Size Bags (10oz) distributed in the U.S. with a production code of 02015748/UPC number 2800010255. No other Nestlé products are impacted.
Nestle asked consumers to contact Nestle Consumer Services directly at 1-800-478-5670 for a full refund and discard any remaining packages. Consumers should NOT return Nestle Raisinets Fun Size Bags (10oz) with a production code of 02015748/UPC number 2800010255 to retailers. Operators are available between 8 a.m. and 8 p.m. EST and after hours for emergencies. Those with questions should contact Nestle Consumer Services at 1-800-478-5670 or via email at mailto:www.nestlecandy@casupport.com.
Thanks!
Cheryl
*Recall* Halloween Candy
There has been a Halloween candy recall....
It looks like certain lots of Mega Pops lollipops are being recalled because the candy may contain "minute traces" of stainless steel.
A consumer complaint prompted North Carolina Department of Agriculture inspectors to test samples of the candy imported from Colombia, and that state agency found metal fibers and flakes in the candy and issued a consumer warning.
Columbina said that they while believe there is no health risk, they still urged customers to return any bag of Mega Pops, REGARDLESS of the lot number, to the store where it was purchasedfor either a refund or store credit.
It looks like the recalled lots of Mega Pops is about 90,000 bags in-total. They were distrubuted nationwide at several retailers and wholesalers.
The RECALLED LOTS are: Watermelon, cherry, orange and grape-flavored lollipops in 14-ounce and 28-ounce cellophane bags with the UPC code numbers of either 0 14272 10873 9 or 0 14272 10862 3. The lot numbers of 1240695, 1209708, or 1209796 can be found in a white square on the back of the bag in the lower left side.
They have setup a 24-hour hotline to answer ANY questions consumers may have. The number is.... (888) 317-3686.
You can go over here for more info.
Thanks!
Cheryl
It looks like certain lots of Mega Pops lollipops are being recalled because the candy may contain "minute traces" of stainless steel.
A consumer complaint prompted North Carolina Department of Agriculture inspectors to test samples of the candy imported from Colombia, and that state agency found metal fibers and flakes in the candy and issued a consumer warning.
Columbina said that they while believe there is no health risk, they still urged customers to return any bag of Mega Pops, REGARDLESS of the lot number, to the store where it was purchasedfor either a refund or store credit.
It looks like the recalled lots of Mega Pops is about 90,000 bags in-total. They were distrubuted nationwide at several retailers and wholesalers.
The RECALLED LOTS are: Watermelon, cherry, orange and grape-flavored lollipops in 14-ounce and 28-ounce cellophane bags with the UPC code numbers of either 0 14272 10873 9 or 0 14272 10862 3. The lot numbers of 1240695, 1209708, or 1209796 can be found in a white square on the back of the bag in the lower left side.
They have setup a 24-hour hotline to answer ANY questions consumers may have. The number is.... (888) 317-3686.
You can go over here for more info.
Thanks!
Cheryl
Tuesday, October 19, 2010
ANOTHER Tylenol Recall
Yes, you read that right. There has been ANOTHER recall by Tylenol. This time, Tylenol is recalling one product lot of Tylenol 8 Hour caplets 50 count bottles. They say that there have been a small number of complaints of a musty or moldy odor that is thought to be caused by the presence of trace amounts of a chemical called 2,4,6-tribromoanisole.
This is a voluntary recall and the state that it is being taken as a precaution, and the risk of adverse medical events is remote.
This is what the package looks like that is being recalled.....
Here is some of the other info for the product too...
NDC Code #
50580-297-50
UPC # 3 0045-0297-51 8
LOT #s
BCM155
So, consumers who purchased product from the lot included in this recall should stop using the product and contact McNeil Consumer Healthcare, either at http://www.tylenol.com/ or by calling 1-888-222-6036 (Monday-Friday 8 a.m. to 8 p.m. Eastern Time, and Saturday-Sunday 9 a.m. to 5 p.m. Eastern Time) for instructions about receiving a refund or product coupon. Consumers who have medical concerns or questions should contact their healthcare provider.
Any adverse reactions may also be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
You can go over here to get more info on the recall.
Thanks!
Cheryl
This is a voluntary recall and the state that it is being taken as a precaution, and the risk of adverse medical events is remote.
This is what the package looks like that is being recalled.....
Here is some of the other info for the product too...
NDC Code #
50580-297-50
UPC # 3 0045-0297-51 8
LOT #s
BCM155
So, consumers who purchased product from the lot included in this recall should stop using the product and contact McNeil Consumer Healthcare, either at http://www.tylenol.com/ or by calling 1-888-222-6036 (Monday-Friday 8 a.m. to 8 p.m. Eastern Time, and Saturday-Sunday 9 a.m. to 5 p.m. Eastern Time) for instructions about receiving a refund or product coupon. Consumers who have medical concerns or questions should contact their healthcare provider.
Any adverse reactions may also be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
You can go over here to get more info on the recall.
Thanks!
Cheryl
Monday, October 18, 2010
Veggie **RECALL**
The Pictsweet Company of Bells, Tennesse has issued a voluntary recall on packages of frozen vegetables sold by Wal-Mart nationwide and Kroger stores in the Southeast, as they may contain glass fragments.
So far, there have been no reports of injuries, but the Pictsweet Co. of Bells, Tennessee, is advising the public not to eat the recalled store-brand vegetables because of the potential for harm.
Consumers should return them to the place of purchase for a full refund.
Here is a list of the recalled vegetables:
-- Kroger 12-ounce Green Peas (UPC 11110 89736). Production Codes of 1440BU, 1440BV, 1440BW, and 1600BD
-- Kroger 12-ounce Peas and Carrots (UPC 11110 89741). Production Codes of 1960BD and 1960BE
-- Great Value 12-ounce Steamable Sweet Peas (UPC 78742 08369). Best by dates of July 20, 2012; July 21, 2012
-- Great Value 12-ounce Steamable Mixed Vegetables (UPC 78742 08026). Best by date of July 15, 2012
Consumers with questions may contact Pictsweet toll-free at 1-800-367-7412, extension 417, from 9 a.m. to 5 p.m. Central Daylight Time, Monday through Friday.
Thanks!
Cheryl
So far, there have been no reports of injuries, but the Pictsweet Co. of Bells, Tennessee, is advising the public not to eat the recalled store-brand vegetables because of the potential for harm.
Consumers should return them to the place of purchase for a full refund.
Here is a list of the recalled vegetables:
-- Kroger 12-ounce Green Peas (UPC 11110 89736). Production Codes of 1440BU, 1440BV, 1440BW, and 1600BD
-- Kroger 12-ounce Peas and Carrots (UPC 11110 89741). Production Codes of 1960BD and 1960BE
-- Great Value 12-ounce Steamable Sweet Peas (UPC 78742 08369). Best by dates of July 20, 2012; July 21, 2012
-- Great Value 12-ounce Steamable Mixed Vegetables (UPC 78742 08026). Best by date of July 15, 2012
Consumers with questions may contact Pictsweet toll-free at 1-800-367-7412, extension 417, from 9 a.m. to 5 p.m. Central Daylight Time, Monday through Friday.
Thanks!
Cheryl
Thursday, September 23, 2010
**Recall** Similac Formula
If you have a little one that presently drinks Similac formula, be aware that Similac just released a voluntary recall of certain Similac-brand infant powder formulas. Let me first start off with that the site is running VERY VERY slow.
Why is Abbott recalling these products?
An internal quality review detected the remote possibility of the presence of a small common beetle in the product produced in one production area in a single manufacturing facility. The United States Food and Drug Administration (FDA) has determined that while the formula containing these beetles poses no immediate health risk, there is a possibility that infants who consume formula containing the beetles or their larvae, could experience symptoms of gastrointestinal discomfort and refusal to eat as a result of small insect parts irritating the GI tract. If these symptoms persist for more than a few days, a physician should be consulted.
What Similac powder infant formulas are being recalled?
* Certain Similac powder product lines offered in plastic containers.
* Certain Similac powder product lines offered in 8-ounce, 12.4-ounce and 12.9-ounce cans.
* To immediately find out if the product in your possession is included in this recall, click here (you will need to type in your lot number to determine if the product is affected) or you can also call 800-986-8850.
No Abbott liquid infant formulas are impacted. Products not involved in the recall include all Abbott Nutrition liquid ready-to-feed and concentrated infant formulas and all powder and liquid specialty formulas, such as Similac Expert Care™ Alimentum®, Elecare ®, Similac Expert Care™ Neosure ®, Similac® Human Milk Fortifier, and metabolic formulas for inherited disorders.
What do I do if I have an affected product?
* Click here or call Abbott’s consumer hotline 800-986-8850, 24 hours a day, seven days a week
* Both the website and the consumer hotline have specific details on how to complete the return process.
**Hip2Save is also reproting that the phone hotline has an extremely long wait.
Thanks Hip2Save!
Cheryl
Why is Abbott recalling these products?
An internal quality review detected the remote possibility of the presence of a small common beetle in the product produced in one production area in a single manufacturing facility. The United States Food and Drug Administration (FDA) has determined that while the formula containing these beetles poses no immediate health risk, there is a possibility that infants who consume formula containing the beetles or their larvae, could experience symptoms of gastrointestinal discomfort and refusal to eat as a result of small insect parts irritating the GI tract. If these symptoms persist for more than a few days, a physician should be consulted.
What Similac powder infant formulas are being recalled?
* Certain Similac powder product lines offered in plastic containers.
* Certain Similac powder product lines offered in 8-ounce, 12.4-ounce and 12.9-ounce cans.
* To immediately find out if the product in your possession is included in this recall, click here (you will need to type in your lot number to determine if the product is affected) or you can also call 800-986-8850.
No Abbott liquid infant formulas are impacted. Products not involved in the recall include all Abbott Nutrition liquid ready-to-feed and concentrated infant formulas and all powder and liquid specialty formulas, such as Similac Expert Care™ Alimentum®, Elecare ®, Similac Expert Care™ Neosure ®, Similac® Human Milk Fortifier, and metabolic formulas for inherited disorders.
What do I do if I have an affected product?
* Click here or call Abbott’s consumer hotline 800-986-8850, 24 hours a day, seven days a week
* Both the website and the consumer hotline have specific details on how to complete the return process.
**Hip2Save is also reproting that the phone hotline has an extremely long wait.
Thanks Hip2Save!
Cheryl
Friday, August 20, 2010
**ANOTHER EGG RECALL**
Yep, you read that right. There was just another egg recall that was announced today.
Iowa's Hillandale Farms said Friday it was recalling its eggs after laboratory tests confirmed illnesses associated with them.
Iowa's Hillandale Farms said Friday it was recalling its eggs after laboratory tests confirmed illnesses associated with them. The company did not say how many eggs were being recalled or if it is connected to Wright County Egg, the other Iowa farm that recalled 380 million eggs earlier this week.
It looks like the eggs were distributed to grocery distribution centers, retail groceries and food service companies which service or are located in fourteen states, including Arkansas, California, Iowa, Illinois, Indiana, Kansas, Minnesota, Missouri, Nebraska, North Dakota, Ohio, South Dakota, Texas, and Wisconsin.
You can go on over here to read the full article.
Thanks!
Cheryl
Iowa's Hillandale Farms said Friday it was recalling its eggs after laboratory tests confirmed illnesses associated with them.
Iowa's Hillandale Farms said Friday it was recalling its eggs after laboratory tests confirmed illnesses associated with them. The company did not say how many eggs were being recalled or if it is connected to Wright County Egg, the other Iowa farm that recalled 380 million eggs earlier this week.
It looks like the eggs were distributed to grocery distribution centers, retail groceries and food service companies which service or are located in fourteen states, including Arkansas, California, Iowa, Illinois, Indiana, Kansas, Minnesota, Missouri, Nebraska, North Dakota, Ohio, South Dakota, Texas, and Wisconsin.
You can go on over here to read the full article.
Thanks!
Cheryl
Wednesday, August 18, 2010
**EGG RECALL**
Wright Country Eggs are issuing a nationwide voluntary recall on their eggs (shell eggs) becuase of possibly being contaminated with Salmonella. It looks like these eggs are packaged under some of the following brand names:
The eggs are packed in varying sizes of cartons (6-egg cartons, dozen egg cartons, 18-egg cartons) with "Julian" dates ranging from 136 to 225 and plant numbers 1026, 1413 and 1946.
Dates and codes can be found stamped on the end of the egg carton. The plant number begins with the letter P and then the number. The "Julian" date follows the plant number, for example: P-1946 223.
Go on over here to get more info.
Thanks Ry!
Cheryl
Lucerne
Albertsons
Mountain Dairy
Ralph’s
Boomsma’s
Sunshine
Hillandale
Trafficanda
Farm Fresh
Shoreland
Lund
Dutch Farms
Kemps
The eggs are packed in varying sizes of cartons (6-egg cartons, dozen egg cartons, 18-egg cartons) with "Julian" dates ranging from 136 to 225 and plant numbers 1026, 1413 and 1946.
Dates and codes can be found stamped on the end of the egg carton. The plant number begins with the letter P and then the number. The "Julian" date follows the plant number, for example: P-1946 223.
Go on over here to get more info.
Thanks Ry!
Cheryl
Friday, July 9, 2010
ANOTHER Tylenol Recall!
Tylenol has announced ANOTHER recall!
This is from their website:.....
MCNEIL CONSUMER HEALTHCARE ANNOUNCES VOLUNTARY RECALL OF CERTAIN OVER-THE-COUNTER (OTC) PRODUCTS IN THE UNITED STATES, FIJI, GUATEMALA, DOMINICAN REPUBLIC, PUERTO RICO, TRINIDAD & TOBAGO, AND JAMAICA
FORT WASHINGTON, PA (July 8, 2010) – McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling 21 lots of over-the-counter medicines. The lots involved, listed below, are sold in the United States, Fiji, Guatemala, Dominican Republic, Puerto Rico, Trinidad & Tobago, and Jamaica. This action is a follow-up to a product recall that McNeil Consumer Healthcare originally announced on January 15, 2010, which was initiated following consumer complaints of a musty or moldy odor, which has been linked to the presence of trace amounts of a chemical called 2,4,6-tribromoanisole (TBA). The risk of serious adverse medical events is remote. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration (FDA).
These lots are being added to the list of recalled products as a precautionary measure after a continuing internal review determined that some packaging materials used in the lots had been shipped and stored on the same type of wooden pallet that was tied to the presence of TBA in earlier recalled lots. All lots involved in the recall were produced before the January 15, 2010 recall, after which McNeil stopped accepting shipments of materials from its suppliers on that type of pallet.
Consumers who purchased product from the lots included in this recall should stop using the product and contact McNeil Consumer Healthcare for instructions on a refund or replacement. For these instructions, and information regarding how to return or dispose of the product, consumers should log on to the internet at http://www.mcneilproductrecall.com/ or call 1-888-222-6036 (Monday-Friday 8 a.m. to 8 p.m. Eastern Time, and Saturday-Sunday 9 a.m. to 5 p.m. Eastern Time). Consumers who have medical concerns or questions should contact their healthcare provider.
Any adverse reactions may also be reported to the FDA’s MedWatch Program by fax at 1-800-FDA-0178, by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch website at www.fda.gov/safety/medwatch/default.htm.
The product lot numbers for the recalled products can be found on the side of the bottle label.
FULL RECALLED PRODUCT LIST:
Product Name Lot Number UPC Code
BENADRYL® ALLERGY ULTRATAB™
BENADRYL® ALLERGY ULTRATAB™ TABLETS 100 count ABA567 312547170338
BENADRYL® ALLERGY ULTRATAB™ TABLETS 100 count ABA574 312547170338
Children’s TYLENOL® Meltaways
CHILDREN’S TYLENOL® MELTAWAYS BUBBLEGUM 30 count ABA544 300450519306
MOTRIN® IB
MOTRIN® IB CAPLET 24 count ACA003 300450481030
MOTRIN® IB CAPLET bonus pack 50+25 count ACA002 300450481764
MOTRIN® IB TABLET 100 count AFA060 300450463043
TYLENOL®, Extra Strength
TYLENOL®, Extra Strength EZ TABLET 225 count ASA206 300450422378
TYLENOL®, Extra Strength EZ TABLET 50 count ABA005 300450422507
TYLENOL®, Extra Strength COOL CAPLET 24 count ABA566 300450444240
TYLENOL®, Extra Strength CAPLET bonus pack 24+12 count ACA025 300450444318
TYLENOL®, Extra Strength CAPLET 50 count AFA018 300450449078
TYLENOL®, Extra Strength CAPLET 50 count
(included in Day/Night Pack) ABA168 300450444530
TYLENOL®, Day & Night Value Pack
(contains Extra Strength CAPLET 50 count
Lot # ABA168 & UPC 300450444530) AEC005 300450527103
TYLENOL®, Day & Night Value Pack
(contains Extra Strength CAPLET 50 count
Lot # ABA168 & UPC 300450444530) AFC005 300450527103
TYLENOL®, Day & Night Value Pack
(contains Extra Strength CAPLET 50 count
Lot # ABA168 & UPC 300450444530) ADC002 300450527103
TYLENOL®, Extra Strength RAPID RELEASE GELCAP 24 count ACA024 300450488244
TYLENOL®, Extra Strength RAPID RELEASE GELCAP 225 count AJA119 300450488251
TYLENOL® PM
TYLENOL® PM CAPLET 24 count ACA005 300450482242
TYLENOL® PM CAPLET 24 count ADA259 300450482242
TYLENOL® PM GELTAB 50 count AFA100 300450176509
TYLENOL® PM RAPID RELEASE GELCAP 20 count ACA004 300450244208
Go over here to get the info that you need.
Thanks Rose Knows Coupons!
This is from their website:.....
MCNEIL CONSUMER HEALTHCARE ANNOUNCES VOLUNTARY RECALL OF CERTAIN OVER-THE-COUNTER (OTC) PRODUCTS IN THE UNITED STATES, FIJI, GUATEMALA, DOMINICAN REPUBLIC, PUERTO RICO, TRINIDAD & TOBAGO, AND JAMAICA
FORT WASHINGTON, PA (July 8, 2010) – McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling 21 lots of over-the-counter medicines. The lots involved, listed below, are sold in the United States, Fiji, Guatemala, Dominican Republic, Puerto Rico, Trinidad & Tobago, and Jamaica. This action is a follow-up to a product recall that McNeil Consumer Healthcare originally announced on January 15, 2010, which was initiated following consumer complaints of a musty or moldy odor, which has been linked to the presence of trace amounts of a chemical called 2,4,6-tribromoanisole (TBA). The risk of serious adverse medical events is remote. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration (FDA).
These lots are being added to the list of recalled products as a precautionary measure after a continuing internal review determined that some packaging materials used in the lots had been shipped and stored on the same type of wooden pallet that was tied to the presence of TBA in earlier recalled lots. All lots involved in the recall were produced before the January 15, 2010 recall, after which McNeil stopped accepting shipments of materials from its suppliers on that type of pallet.
Consumers who purchased product from the lots included in this recall should stop using the product and contact McNeil Consumer Healthcare for instructions on a refund or replacement. For these instructions, and information regarding how to return or dispose of the product, consumers should log on to the internet at http://www.mcneilproductrecall.com/ or call 1-888-222-6036 (Monday-Friday 8 a.m. to 8 p.m. Eastern Time, and Saturday-Sunday 9 a.m. to 5 p.m. Eastern Time). Consumers who have medical concerns or questions should contact their healthcare provider.
Any adverse reactions may also be reported to the FDA’s MedWatch Program by fax at 1-800-FDA-0178, by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch website at www.fda.gov/safety/medwatch/default.htm.
The product lot numbers for the recalled products can be found on the side of the bottle label.
FULL RECALLED PRODUCT LIST:
Product Name Lot Number UPC Code
BENADRYL® ALLERGY ULTRATAB™
BENADRYL® ALLERGY ULTRATAB™ TABLETS 100 count ABA567 312547170338
BENADRYL® ALLERGY ULTRATAB™ TABLETS 100 count ABA574 312547170338
Children’s TYLENOL® Meltaways
CHILDREN’S TYLENOL® MELTAWAYS BUBBLEGUM 30 count ABA544 300450519306
MOTRIN® IB
MOTRIN® IB CAPLET 24 count ACA003 300450481030
MOTRIN® IB CAPLET bonus pack 50+25 count ACA002 300450481764
MOTRIN® IB TABLET 100 count AFA060 300450463043
TYLENOL®, Extra Strength
TYLENOL®, Extra Strength EZ TABLET 225 count ASA206 300450422378
TYLENOL®, Extra Strength EZ TABLET 50 count ABA005 300450422507
TYLENOL®, Extra Strength COOL CAPLET 24 count ABA566 300450444240
TYLENOL®, Extra Strength CAPLET bonus pack 24+12 count ACA025 300450444318
TYLENOL®, Extra Strength CAPLET 50 count AFA018 300450449078
TYLENOL®, Extra Strength CAPLET 50 count
(included in Day/Night Pack) ABA168 300450444530
TYLENOL®, Day & Night Value Pack
(contains Extra Strength CAPLET 50 count
Lot # ABA168 & UPC 300450444530) AEC005 300450527103
TYLENOL®, Day & Night Value Pack
(contains Extra Strength CAPLET 50 count
Lot # ABA168 & UPC 300450444530) AFC005 300450527103
TYLENOL®, Day & Night Value Pack
(contains Extra Strength CAPLET 50 count
Lot # ABA168 & UPC 300450444530) ADC002 300450527103
TYLENOL®, Extra Strength RAPID RELEASE GELCAP 24 count ACA024 300450488244
TYLENOL®, Extra Strength RAPID RELEASE GELCAP 225 count AJA119 300450488251
TYLENOL® PM
TYLENOL® PM CAPLET 24 count ACA005 300450482242
TYLENOL® PM CAPLET 24 count ADA259 300450482242
TYLENOL® PM GELTAB 50 count AFA100 300450176509
TYLENOL® PM RAPID RELEASE GELCAP 20 count ACA004 300450244208
Go over here to get the info that you need.
Thanks Rose Knows Coupons!
Friday, June 25, 2010
**Kellogg's Cereal Recall**
Kellogg’s just issued a voluntarily recall of select packages of Kellogg’s Corn Pops, Honey Smacks, Froot Loops and Apple Jacks cereals. You should NOT eat the recalled products because they do not meet quality standards…The cereal was recalled due to the fact an off-flavor and smell was coming from the bag. Apparently, Kellogg’s has identified a substance in the package liners that can produce an uncharacteristic waxy-like off taste and smell.
Below is a list of the recalled cereals:
(NOTE: Only products with the letters "KN" following the Better If Used Before Date are included in the recall. Products with a "KM" designation are NOT included in the recall. In addition, no products in Canada are affected.)
Kellogg’s® Apple Jacks®
UPC 3800039136
17 ounce package with Better if Used Before Dates between APR 10 2011 and JUN 22 2011
UPC 3800039132 3
8.7 ounce packages with Better if Used Before Dates between JUN 03 2011 and JUN 22 2011
Kellogg’s® Corn Pops®
UPC 3800039109
12.5 ounce packages with Better if Used Before Dates between MAR 26 2011 and JUN 22 2011
UPC 3800039111
17.2 ounce packages with Better if Used Before Dates between MAR 26 2011 and JUN 22 2011
UPC 3800039116
9.2 ounce packages with Better if Used Before Dates between APR 05 2011 and JUN 22 2011
Kellogg’s® Froot Loops®
UPC 3800039118
12.2 ounce packages with Better if Used Before Dates between MAR 26 2011 and JUN 22 2011
UPC 3800039120
17 ounce packages with Better if Used Before Dates between MAR 26 2011 and JUN 22 2011
UPC 3800039125
8.7 ounce packages with Better if Used Before Dates between MAR 26 2011 and JUN 22 2011
Kellogg’s®Honey Smacks®
UPC 3800039103
15.3 ounce packages with Better if Used Before Dates between MAR 26 2011 and JUN 22 2011
**For those with questions or who would like a replacement may contact the Kellogg Consumer Response Center at 888-801-4163 from 8 am to 8 pm Eastern time. Go here for more information.
Thanks for the heads up on this Hip 2 Save!
Cheryl
Friday, June 4, 2010
***RECALL*** MCDONALD'S SHREK GLASSES!
Cadmium has been discovered in the painted design on Shrek-themed drinking glasses being sold nationwide at McDonald's, forcing them to recall the glasses.
The U.S. Consumer Product Safety Commission warned consumers to immediately stop using the glasses. McDonald's said it would post instructions on its website next week regarding refunds.
Go here to get more information on the recall.
Thanks!
Cheryl
The U.S. Consumer Product Safety Commission warned consumers to immediately stop using the glasses. McDonald's said it would post instructions on its website next week regarding refunds.
Go here to get more information on the recall.
Thanks!
Cheryl
Tuesday, May 11, 2010
Lettuce Recall
This has only affected certain states, but just recently they have expanded the recall to a few more states. Here are a couple of articles that have some great info for you. Go here to the Freshway Foods Website and/or go here to the Comcast story.
Thanks!
Cheryl
Thanks!
Cheryl
Thursday, May 6, 2010
REPOST **Children's Tylenol Recall As Well As** .........
Children's Motrin, Children's Zyrtec, Children's Benadryl. Go ahead and click on this link and you will be able to see specifics as to what is recalled.
This is taken from their website.....
McNeil Consumer Healthcare is initiating this voluntary recall because some of these products may not meet required quality standards. This recall is not being undertaken on the basis of adverse medical events.
However, as a precautionary measure, parents and caregivers should not administer these products to their children.
Please see our FAQs for actions that can be taken if you have product affected by this recall and for information on disposing of these over-the-counter medications.
Our Consumer Care Center is available to answer your general questions about this recall and provide information about receiving a coupon or refund for recalled products. If you have health concerns, please talk to your healthcare provider. You can contact us either by phone at 888-222-6036, email or request to have us call you back per the options below. Due to high call volume, it may take longer than normal to get through to our live call center. You may also use one of the other options below and we will get back to you. Again, click here to email us, click here to request a call back or call 888-222-6036.
I know the picture is not all that great, but that is as big as I could get it. You can also get the list here.
Thanks!
Cheryl
This is taken from their website.....
McNeil Consumer Healthcare is initiating this voluntary recall because some of these products may not meet required quality standards. This recall is not being undertaken on the basis of adverse medical events.
However, as a precautionary measure, parents and caregivers should not administer these products to their children.
Please see our FAQs for actions that can be taken if you have product affected by this recall and for information on disposing of these over-the-counter medications.
Our Consumer Care Center is available to answer your general questions about this recall and provide information about receiving a coupon or refund for recalled products. If you have health concerns, please talk to your healthcare provider. You can contact us either by phone at 888-222-6036, email or request to have us call you back per the options below. Due to high call volume, it may take longer than normal to get through to our live call center. You may also use one of the other options below and we will get back to you. Again, click here to email us, click here to request a call back or call 888-222-6036.
I know the picture is not all that great, but that is as big as I could get it. You can also get the list here.
Thanks!
Cheryl
Monday, April 19, 2010
Ground Beef Recall at ALL Winco Stores
WinCo has expanded its hamburger recall to include ground beef sold at its 70 stores in California, Nevada, Idaho, Washington, Oregon and Utah. They have found some meat tainted with an E. coli bacteria that causes foodborne illness. The recall time-frame is expanded to include fresh hamburger packed in Styrofoam trays with a sale date of March 28 through April 9.
This if from their website....
Recall notice: All fresh ground beef packed in styrofoam trays with a sale date of March 28, 2010 through April 9, 2010 purchased from our Meat Departments at any of our stores should be destroyed or returned for full refund. DO NOT USE OR FREEZE.
Go here to get more info.....
Thanks!
Cheryl
This if from their website....
Recall notice: All fresh ground beef packed in styrofoam trays with a sale date of March 28, 2010 through April 9, 2010 purchased from our Meat Departments at any of our stores should be destroyed or returned for full refund. DO NOT USE OR FREEZE.
Go here to get more info.....
Thanks!
Cheryl
Thursday, January 21, 2010
This is thanks to Hip 2 Save ......................
Over 630,000 cribs are being recalled by Dorel-Asia. Apparantly the drop side hardware can fail causing the drop side to detach from the crib. When the drop side detaches it creates a space in which an infant or toddler can become entrapped and suffocate or strangle.
The cribs that are part of this recall were sold at K-Mart, Walmart and Sears stores nationwide from January 2005 to December 2009. You can go here to see the Press Release and the model numbers and pictures of the cribs included in this recall.
If your crib is in fact part of the recall, then you should immediately stop using the crib, find an alternative safe sleeping environment for your child, and contact Dorel Asia to receive a free replacement kit. Consumers should log on to http://www.dorel-asia.com/crib-safety-notice or call the Dorel Asia toll-free at (866) 762-2304 between 8 a.m. and 4:30 p.m. ET Monday through Friday to order the free replacement kit to prevent child entrapment in these cribs. The repair kits will be provided to owners within the next several weeks.
NEW UPDATE: There is also a huge recall on Graco Strollers! You can check out the Press Release here.
Thanks.
Cheryl
Over 630,000 cribs are being recalled by Dorel-Asia. Apparantly the drop side hardware can fail causing the drop side to detach from the crib. When the drop side detaches it creates a space in which an infant or toddler can become entrapped and suffocate or strangle.
The cribs that are part of this recall were sold at K-Mart, Walmart and Sears stores nationwide from January 2005 to December 2009. You can go here to see the Press Release and the model numbers and pictures of the cribs included in this recall.
If your crib is in fact part of the recall, then you should immediately stop using the crib, find an alternative safe sleeping environment for your child, and contact Dorel Asia to receive a free replacement kit. Consumers should log on to http://www.dorel-asia.com/crib-safety-notice or call the Dorel Asia toll-free at (866) 762-2304 between 8 a.m. and 4:30 p.m. ET Monday through Friday to order the free replacement kit to prevent child entrapment in these cribs. The repair kits will be provided to owners within the next several weeks.
NEW UPDATE: There is also a huge recall on Graco Strollers! You can check out the Press Release here.
Thanks.
Cheryl
Tuesday, January 19, 2010
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