Food and Drug Administration Recall Published Jan. 26, 2010 By A1C Lynsie Lorenz 374th Airlift Wing Public Affairs YOKOTA AB, Japan -- The Food and Drug Administration (FDA) recently recalled several over the counter drug products that may have been contaminated with tribromoanisole (TBA). TBA causes the product to have a moldy or musty smell and in some cases can cause nausea if ingested. The products that have been recalled from Yokota Air Base are as follows: Jr. Strength Motrin orange chewable tablet 24 count Tylenol Extra Strength EZ tablet 50 count Tylenol Rapid Release gel 50 count Motrin IB caplet 100 count Motrin IB tablet 24 count St. Joseph's Aspirin Enteric tablet 36 count Tylenol PM Extra Strength caplet 50 count Tylenol PM Extra Strength caplet 100 count Rolaids Antacid Tabs original peppermint 150 count The 374 MDG pharmacy does not stock and has not dispensed these specific products. The pharmacy has directions available for destroying unwanted medication. Patients can just stop by the pharmacy window and ask for a flier. If you have recently purchased these products, DON'T USE THESE! Either discard them or return them to the BX or Shoppette promptly. Any questions or concerns, please contact Public Health's Food Safety Office at 225-4360 or 4361. For more information about this recall and a complete listing of other products not sold here at Yokota, please visit http://www.fda.gov/Safety/Recalls/ucm197746.htm