Where is more info pertaining to Tylenol Recall 2009 Expanded?
In consultation with the U.S. Food and Drug Administration (FDA), McNeil Consumer Healthcare, a Division of McNEIL-PPC, Inc., is voluntarily recalling all currently available bottles of TYLENOL Arthritis Pain Caplet 100 count. These bottles can be easily identified by a distinctive red EZ-OPEN CAP. In November 2009, 5 lots of this product were recalled due to consumer reports of an unusual moldy, musty, or mildew-like odor that was associated with nausea, stomach pain, vomiting and diarrhea. The recall is being expanded, as a precaution, to include all TYLENOL Arthritis Pain Caplet 100 count bottles with the distinctive red EZ-OPEN CAP. Only the TYLENOL Arthritis Pain Caplet 100’s are affected by this action. All other TYLENOL Arthritis Pain products remain available. McNeil Consumer Health care will reintroduce the TYLENOL Arthritis Pain Caplet 100 count product by January, 2010.
