Tylenol
Recall of tylenol cold Liquid Products
November 24, 2010 - In consultation with the U.S. Food and Drug Administration (FDA), McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling, from the wholesale and retail level, three TYLENOL® Cold Multi-Symptom liquid products in order to update the labeling for these products. The specific products involved, listed below, are sold in the United States.
This is a wholesale and retail level recall and is not being undertaken on the basis of adverse events. No action is required by consumers or healthcare providers and consumers can continue to use the product.
McNeil Consumer Healthcare initiated the recall after an internal review revealed that information about the presence of alcohol from flavoring agents was noted as an inactive ingredient listed on the package, but not on the front panel of the product. Certain flavoring agents contribute small (< 1%) amounts of alcohol.
Consumers with questions should call our Consumer Care Center at 1-888-222-6036 (available Monday-Friday from 8 a.m. - 8 p.m. ET and Saturday - Sunday, 9 a.m. - 5 p.m. Eastern Time.)
The NDC codes for the recalled products can be found on the product front panel.
Source : FDA
Link to Source
Tylenol Recall 2010 Lot Numbers –
The recall of Tylenol and other over-the-counter medicines has explicitly grown again with the Tylenol maker McNeil PCC Inc. said and announces today the recall of 21 lots of medicines as a measure.
In fact, a Tylenol recall issued last year by the Johnson & Johnson unit of McNeil Consumer Healthcare because of chemical contamination has been expanded for a second time to include Benadryl Allergy Ultratablets and Extra Strength Tylenol.
And for today, recall of Tylenol also includes various formulas like the children’s Tylenol and Motrin. Apparently, the latest recall also includes Benadryl Allegry Ultratab tablets in 100 counts bottles sold in the US.
“McNeil should have acted faster,” said Deborah Autor, director of the FDA’s Office of Compliance, of the arm of Johnson & Johnson that manufactures Tylenol products. “When something smells bad, literally or figuratively, they must aggressively investigate and solve the problem.”
Below are the lists ofTylenol recall 2010 lot numbers:
LINK TO SOURCE
November 24, 2010 - In consultation with the U.S. Food and Drug Administration (FDA), McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling, from the wholesale and retail level, three TYLENOL® Cold Multi-Symptom liquid products in order to update the labeling for these products. The specific products involved, listed below, are sold in the United States.
This is a wholesale and retail level recall and is not being undertaken on the basis of adverse events. No action is required by consumers or healthcare providers and consumers can continue to use the product.
McNeil Consumer Healthcare initiated the recall after an internal review revealed that information about the presence of alcohol from flavoring agents was noted as an inactive ingredient listed on the package, but not on the front panel of the product. Certain flavoring agents contribute small (< 1%) amounts of alcohol.
Consumers with questions should call our Consumer Care Center at 1-888-222-6036 (available Monday-Friday from 8 a.m. - 8 p.m. ET and Saturday - Sunday, 9 a.m. - 5 p.m. Eastern Time.)
The NDC codes for the recalled products can be found on the product front panel.
Source : FDA
Link to Source
Tylenol Recall 2010 Lot Numbers –
The recall of Tylenol and other over-the-counter medicines has explicitly grown again with the Tylenol maker McNeil PCC Inc. said and announces today the recall of 21 lots of medicines as a measure.
In fact, a Tylenol recall issued last year by the Johnson & Johnson unit of McNeil Consumer Healthcare because of chemical contamination has been expanded for a second time to include Benadryl Allergy Ultratablets and Extra Strength Tylenol.
And for today, recall of Tylenol also includes various formulas like the children’s Tylenol and Motrin. Apparently, the latest recall also includes Benadryl Allegry Ultratab tablets in 100 counts bottles sold in the US.
“McNeil should have acted faster,” said Deborah Autor, director of the FDA’s Office of Compliance, of the arm of Johnson & Johnson that manufactures Tylenol products. “When something smells bad, literally or figuratively, they must aggressively investigate and solve the problem.”
Below are the lists ofTylenol recall 2010 lot numbers:
- TYLENOL®, Extra Strength EZ TABLET 225 count (ASA206)
- TYLENOL®, Extra Strength EZ TABLET 50 count (ABA005)
- TYLENOL®, Extra Strength COOL CAPLET 24 count (ABA566)
- TYLENOL®, Extra Strength CAPLET bonus pack 24+12 count (ACA025)
- TYLENOL®, Extra Strength CAPLET 50 count (AFA018)
- TYLENOL®, Day & Night Value Pack (AEC005)
- TYLENOL®, Extra Strength RAPID RELEASE GELCAP 24 count (ACA024)
- TYLENOL®, Extra Strength RAPID RELEASE GELCAP 225 count (AJA119)
LINK TO SOURCE