It seems that there is a pretty big problem when Johnson and Johnson Tylenol manufacturers decide to stack empty pill bottles on wooden pallets treated with the fungicide 2,4,6-tribromophenol. Somehow, the fungicide actually makes its way into the pill bottles and contaminates the Tylenol. Now McNeil knows this is a problem as it has happened 13 times! I told you about one of the recalls earlier this year so aren't we all like, "Hello, earth to McNeil and Johnson & Johnson...do you think you may have a problem?"
ABC News Video from January of 2010
So once again on October 18, 2010, McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling one product lot of TYLENOL® 8 Hour caplets 50 count bottles. Like the with the other recalls, McNeil is taking this action following a small number of complaints of a musty or moldy odor. The uncharacteristic odor is thought to be caused by the presence of trace amounts of 2,4,6-tribromoanisole.
McNeil says that this voluntary action is being taken as a precaution and the risk of adverse medical events is remote. But thankfully maybe they are trying to stay on top of it because they are facing a US Congressional investigation stemming from quality control issues from an earlier recall. People have gotten sick although, to date, observed events reported to McNeil for this lot were temporary and non-serious. I sure don't want to be one of the sickened do you? There is a lawyer running around who is helping people to sue McNeil for becoming ill from the fungus tainted Tylenol.
FULL RECALLED PRODUCT LIST:
The product lot number for the recalled caplets can be found on the side of the bottle label.
Consumers who purchased product from the lot included in this recall should stop using the product and contact McNeil Consumer Healthcare, either at www.tylenol.com9 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.
P.S.- I am really glad that you stopped by our Environmental Booty Blog and I hope you have learned or shared a thing or two. I hope that , now that you've found us, you won't lose us! You can join our green living online community, subscribe to our posts, download our community toolbar, Tweet with me on Twitter or Come Shop with Me to stay in touch! - Shane :)