American Health Ranitidine Tablet Recall [US]

American Health Ranitidine Tablet Recall [US]

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US FlagUS/Silver Spring: American Health Packaging, a Columbus, Ohio establishment, recalls eleven (11) lots of Ranitidine Tablets, USP 150 mg, 100 count Unit Dose Blisters from the American marketplace due to suspected levels of N-Nitrosodimethylamine (“NDMA”), a probable Human Carcinogen, above the allowable limits established by the FDA and consequential risk of Cancer, all serious health hazards.


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Additional information:
The US Food and Drug Administration (“FDA”) reports the following prescription drug products are subject to this recall:

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