FDAMarch 11, 2021drug

Omeprazole Delayed-Release Capsules, USP, 20 mg, 1000 count bottles, Rx Only, distributed by Breckenridge Pharmaceutical, Inc., Berlin, CT, Manufactured by Tow Pharmaceutical Europe, S.L., Martorelles (Barcelona), Spain NDC 51991-643-10

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Failed Impurities/Degradation Specifications: Out-of-Specification results obtained for unknown impurities during stability testing.

What to do

FDA enforcement status: Terminated

Brands named

breckenridge pharmaceuticalbreckenridge

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Omeprazole Delayed-Release Capsules, USP, 20 mg, 1000 count bottles, Rx Only, distributed by Breckenridge Pharmaceutical, Inc., Berlin, CT, Manufactured by Tow Pharmaceutical Europe, S.L., Martorelles (Barcelona), Spain NDC 51991-643-10 — Recall Details · AllClear