240 FDA recalls mention Acetaminophen. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Acetaminophen.
Reason CGMP deviation: product outside labeled storage temperature requirements.
Reason Boxes mislabeled to read "Decongestant Free", but the product contains Phenylephrine HCI 5mg
Reason Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Reason Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Reason Temperature Abuse: Product distributed in refrigerated trucks with labels attached to pallets indicating "Refrigerate Upon Arrival", however product…
Reason CGMP Deviations: product held outside appropriate storage temperature conditions.
Reason CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Reason CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Reason CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Reason CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Reason CGMP Deviations: Failure to properly investigate failed microbial testing.
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations
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