Amerisource Health Services LLC — Primidone Tablets recall — Low risk

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Low risk

The FDA considers this unlikely to cause harm. Return it for a refund if you would rather not keep it.

Class III

Unlikely to cause any adverse health consequence, but the product breaks FDA rules.
Refunds don't require a receipt, and you don't need proof of purchase.
FDA status: Ongoing.

What was recalled

Source: FDA · synced 29 Jul 2026 13:14

Low risk Filed 2026-05-27

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

Primidone Tablets, USP, 50 mg, 100 Tablets (10 x 10 unit dose blister) per carton, Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Carton NDC: 68084-202-01; Individual Dose NDC: 68084-202-11

Check these codes: Lot 1028739, exp 12/31/2027; Lot 1025622, exp 06/30/2027

225,000 tablets · distributed usa nationwide Recall D-0537-2026 on FDA.gov ↗

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One email per recall. Nothing else, ever.