Tylenol Recall, Johnson and Johnson Recall Tylenol Arthritis

12/29/2009-Johnson & Johnson (NYSE:JNJ) is now recalling all product lots of the Arthritis Pain Caplet 100 count bottles with the red EZ-Open Cap, according to a statement on the Food and Drug Administration website.

The recall was implemented due to a moldy odor that can cause stomach pain and nausea caused by trace amounts of the chemical 2, 4, 6-tribromoanisole resulting from the breakdown of another chemical used to treat wooden pallets.

Side effects also include vomiting and diarrhea, but have been “temporary and non-serious.”

All Tylenol Arthritis products, other than the lots specified, remain available.

Previous post:

Next post:

Disclaimer: This content is not intended as a substitute for professional medical/dental advice, diagnosis, or treatment. Always seek the advice of your physician, dental professional, or other qualified health provider with any questions you may have regarding a medical/dental condition. Never disregard professional medical/dental advice or delay in seeking it because of Content found on the Website.