Medline Industries, Inc. Issues A Voluntary Nationwide Recall Of One Lot Of Acetaminophen Tablets, 500mg, Due To Mislabeling With Incorrect Strength

"U.S. Food & Drug Administration (FDA)" <fda@xxxxxxxxxxxxxxxxxxxxxxx> · Thu, 15 Oct 2015 08:23:31 -0500

Title:     Medline Industries, Inc. Issues A Voluntary Nationwide Recall Of One Lot Of Acetaminophen Tablets, 500mg, Due To Mislabeling With Incorrect Strength

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Medline Industries, Inc. Issues A Voluntary Nationwide Recall Of One Lot Of Acetaminophen Tablets, 500mg, Due To Mislabeling With Incorrect Strength
10/14/2015 08:05 PM EDT

Medline Industries, Inc. announced that it will initiate a voluntary nationwide recall of lot # 45810 of Acetaminophen tablets, 500mg, uncoated compressed tablets to the consumer level. The Acetaminophen 500mg, Tab 100/BT (OTC20101) has been found to be mislabeled displaying “Acetaminophen 325mg” (OTC10101) instead of “Acetaminophen 500mg”.

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