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Breckenridge Pharmaceutical recalls - full list & free alerts

6 official U.S. recalls involving Breckenridge Pharmaceutical in the last 12 months, most recently on 2026-06-17.

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Full list (6)

Breckenridge Pharmaceutical, Inc.: Duloxetine Delayed-Release Capsules, USP, 30mg, 1000 Capsule bottles, Rx only, Manufactured. by: Towa Pharmaceutical Europe, S.L. Martorelle
DrugsFDA (drug) · 2026-06-17 · Class II
Breckenridge Pharmaceutical, Inc.: Duloxetine Delayed-Release Capsules, USP, 60mg, packaged in a) 90 Capsules (NDC 51991-748-90); b) 1000 Capsules (51991-748-10), Rx Only, Mfr
DrugsFDA (drug) · 2026-06-17 · Class II
Breckenridge Pharmaceutical, Inc.: Duloxetine Delayed-Release Capsules USP, 60mg, Rx Only, 90-count bottle, Mfr. by Towa Pharmaceutical Eurpoe S.L., Martorelles, (Barcelona),
DrugsFDA (drug) · 2026-05-13 · Class II
Breckenridge Pharmaceutical, Inc.: Duloxetine Delayed-Release Capsules, USP, 60 mg, 1000-Capsule bottles, Rx Only, Manufactured by: Towa Pharmaceuticals Europe, S.L. Marotrell
DrugsFDA (drug) · 2025-12-10 · Class II
Breckenridge Pharmaceutical, Inc.: Duloxetine Delayed-Release Capsules, USP, 60 mg, 1000-Capsule bottles, Rx Only, Manufactured by: Towa Pharmaceuticals Europe, S.L. Marotrell
DrugsFDA (drug) · 2025-12-10 · Class II
Breckenridge Pharmaceutical, Inc.: Duloxetine Delayed-Release Capsules, USP, 60 mg, a.) 90-count bottle (NDC: 51991-748-90), b.)1000-count bottle (NDC 51991-748-10),Rx Only,
DrugsFDA (drug) · 2025-11-05 · Class II