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    Acetaminophen Recall Announced

    About 11 Million Bottles of Store-Brand 500-Milligram Caplets Recalled
    WebMD Health News
    Reviewed by Louise Chang, MD

    Nov. 9, 2006 -- The FDA today announced a recall of about 11 million bottles of store-brand acetaminophen 500-milligram caplets.

    Those caplets are over-the-counter drugs for pain relief and fever reduction. They're sold by about 130 companies, including Wal-Mart, CVS, and other drug stores, grocery stores, and wholesalers.

    The recall is due to "small metal fragments found in a small number of these caplets," states an FDA news release.

    The fragments range in size from "microdots" to 8-millimeter pieces of wire, according to the FDA.

    The FDA and the caplets' maker, Perrigo Company of Allegan, Mich., are investigating how those metal fragments got into the caplets.

    So far, no illnesses, injuries, or consumer complaints have been reported to the FDA or Perrigo, according to the FDA.

    The FDA "believes the probability of serious adverse health consequences is remote," the FDA's Jason Brodsky told reporters in a teleconference.

    Brodsky is the FDA's assistant commissioner for external relations.

    "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," Brodsky says.

    Advice for Consumers

    For a full list of the companies that sell store-brand 500 milligram acetaminophen made by Perrigo, visit the FDA's web site at

    The FDA's web site also lists the recalled batches of the drug. That list is posted at

    The recalled drugs have expiration dates ranging from September 2006 through August 2009.

    The FDA advises consumers who believe they have the recalled acetaminophen to "discontinue use immediately" and call Perrigo's consumer affairs department at (877) 546-0454 for further instructions.

    People who think they may have been harmed by the affected caplets should talk to their doctors, says Brodsky.

    "We believe, at present, that this is a relatively small fraction of the total available acetaminophen on the market," the FDA's Douglas Throckmorton, MD, told reporters in the teleconference. Throckmorton is the deputy director of the FDA's Center for Drug Evaluation and Research.

    Any adverse reactions to the products should be reported to the FDA's MedWatch program, which can be reached by phone at (800) FDA-1088, by fax at (800) FDA-0178, or on the MedWatch web site at

    Adverse reactions should also be reported by phone to Perrigo's consumer affairs department at (877) 546-0454, says the FDA.

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