Bayer Recall Due to Labeling Error
MORRISTOWN, N.J., Dec. 7, 2012 /PRNewswire/ -- In consultation with the U.S. Food and Drug Administration (FDA), Bayer HealthCare's Consumer Care division has begun a voluntary recall of BRONKAID Caplets Dual Action Formula. Bayer initiated the recall after identifying that certain information was inadvertently excluded from the product carton label. It is important to note that this represents a labeling omission only. The quality of the product itself is not affected.
The affected BRONKAID product lot number can be found on both the interior blister package (in black text adjacent to the expiration date) as well as on the exterior carton containing the blister packaging (embossed on the side panel next to the expiration date)
Product Name: BRONKAID Caplets Dual Action Formula Package size/UPC: 24 caplets ( UPC 300240537879) and 60 caplets ( UPC 300240537855) Lot #s: see below list
This product was sold only in the U.S. at retail outlets nationwide.
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Source: http://www.pmpnews.com/news/bayer-consumer-care-voluntarily-recalls-56-lots-bronkaid-caplets-dual-action-formula-due-produc
