In This Section . . .

For Immediate Release: 11/13/06

Nationwide Recall of "Store Brand" 500 mg Acetaminophen Caplets

Perrigo Company of Allegan, Michigan is conducting a voluntary recall of 383 lots of acetaminophen 500mg caplets manufactured and distributed under various store-brands. The recall is being conducted because tiny metal fragments have been found in a small number of these caplets.

Approximately 11 million bottles containing varying quantities of acetaminophen 500mg caplets are affected by the recall. For a list of affected batches, visit: http://www.fda.gov/oc/po/firmrecalls/perrigo/perrigobatchlist.html

Consumers can determine if they are in possession of a recalled product by locating the batch number printed on the container label. For a list of stores that carry store-brands potentially affected by this recall, visit: http://www.fda.gov/oc/po/firmrecalls/perrigo/perrigocustlist.html

To date, there has been no illness or injuries reported related to this problem and no consumer complaints have been reported to the FDA or to Perrigo. Based on information currently available, the FDA believes the probability of serious adverse health consequences is remote; however if a consumer were to swallow an affected caplet, it could result in minor stomach discomfort and/or possible cuts to the mouth or throat. Consumers should consult their physician if they suspect they've been harmed by use of this product.

To view the FDA press release in its entirety, visit: http://www.fda.gov/bbs/topics/NEWS/2006/NEW01507.html

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