How do I know if my Breckenridge Pharmaceutical product is part of a recall?

Compare the lot code, UPC, model number or dates on your product with the official recall notice linked on this page. Our lot/UPC checker searches the official text but is not a guarantee.

What should I do if my Breckenridge Pharmaceutical product is recalled?

Follow the instructions in the official notice from the agency (FDA, USDA FSIS, CPSC or NHTSA), such as stopping use, returning or discarding the product, or contacting the company.

Is Breckenridge Pharmaceutical recalled? 6 official recalls

Official U.S. agency records list 6 recalls involving Breckenridge Pharmaceutical in the last 12 months, most recently on 2026-06-17. Check each official notice for the exact products, lot codes and dates affected.

Check a lot code, UPC or model number

This is not a guarantee; check the official notice.

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

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Is Breckenridge Pharmaceutical recalled?

Recalls (6)