Hydrocodone Bitartrate and Acetaminophen Tablets USP, 10 mg/500 mg, 500-count Tablets per bottle, Rx only, Manufactured By…
Reason Superpotent (Multiple Ingredient) Drug: There is the potential for oversized and superpotent tablets.
Recalls of common over-the-counter and prescription pain relievers.
415 recalls in this category, newest first.
Reason Superpotent (Multiple Ingredient) Drug: There is the potential for oversized and superpotent tablets.
Reason Superpotent (Multiple Ingredient) Drug: Confirmed customer complaints of oversized tablets resulting in superpotent assays of both the hydrocodone…
Reason Presence of Particulate Matter: The firm initiated the recall due to visible presence of particulate matter.
Reason Incorrect/Undeclared Excipients: The firm recalled specific lots of Walgreens brand Aspirin Free Tension Headache Caplets due to the presence of…
Reason Labeling; labeled with incorrect EXP Date; Incorrect expiration date printed on the outer packaging. Package incorrectly states 5/2014 should…
Reason Labeling: Label Mix-Up: Bottles labeled as Naproxen Tablets USP, 500 mg, 100-count may contain 90-count Pravastatin Sodium Tablets, 40 mg.
Reason Impurities/Degradation Products: exceeded specification at 3 month stability testing
Reason Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012 because…
Reason CGMP Deviations: This product is being recalled because expired flavoring was used in the manufacturing of these lots.
Reason Subpotent (Multiple Ingredient) Drug: Low out of specification assay results for the hydrocodone bitartrate ingredient was found.
Reason Adulterated Presence of Foreign Tablets: Customer complaint that some Endocet 10 mg/325 mg tablets were found mixed in a bottle with Endocet 10…
Reason Labeling: Label Mix-up: This recall was initiated after identifying that the label statement on the blister strip regarding the maximum number of…
Reason Labeling: Label Mix-up: This recall was initiated after identifying that the label statement on the blister strip regarding the maximum number of…
Reason Tablet Thickness: Recall was initiated due to the presence of one slightly oversized tablet in a bottle of the identified lot.
Reason Tablet Separation: The manufacturer of Arthrotec had recalled the lots that were used to re-package this product because they may contain broken…
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