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Have there been any recalls on PEPCID Complete?

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Quick Answer

Johnson & Johnson Merck, headquartered in Ft. Washington, Pennsylvania, issued a recall of PEPCID Complete and PECID AC tablets on Aug. 20, 2010, according to the U.S. Federal Drug Enforcement Agency. The recall affected several strengths and bottle counts.

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Full Answer

The recall of PEPCID Complete tablets resulted from a defective container issue, notes the FDA. Inspectors found punctures in a small number of bottles, along the bottom edges. The punctures occurred during the packaging process. The recall affected 50-count bottles of PEPCID Complete tablets in 10-, 165- and 800-milligram doses. Also pulled during the recall were 90-count bottles of 10-milligram PEPCID AC tablets.

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