Title: acetaminophen 500 mg caplets
Birdbomb - November 11, 2006 10:01 AM (GMT)
MedWatch - The FDA Safety Information and Adverse Event Reporting
Program
FDA and Perrigo Company notified the public of a voluntary recall of
383
lots of acetaminophen 500 mg caplets manufactured and distributed under
various store-brands as a result of small metal fragments found in a
small number of these caplets. Consumers can determine if they are in
possession of a recalled product by locating the batch number printed
on
the container label. A list of stores that carry store-brands
potentially affected by this recall, as well as batch numbers affected,
is located on FDA's website (referenced below).
To date, there have been no illness or injuries received 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.
Read the complete MedWatch 2006 Safety Summary, including links to the
FDA News Release, Perrigo Voluntary Product Recall Customer List, and
Perrigo Recalled Batches, at: http://www.fda.gov/medwatch/safety/2006/sa...m#acetaminophen