Breckenridge Pharmaceutical, Inc: 33 recalls on record

Recalls filed with 1 agency: FDA (33).

First recall on record: November 18, 2015. Most recent: June 17, 2026.

Risk classification: Class II: 31 · Class III: 2

Most recent recalls

DateAgencyProduct
June 17, 2026FDADuloxetine Delayed-Release Capsules, USP, 60mg, packaged in a) 90 Capsules (NDC 51991-748…D-0583-2026
June 17, 2026FDADuloxetine Delayed-Release Capsules, USP, 30mg, 1000 Capsule bottles, Rx only, Manufactur…D-0582-2026
May 13, 2026FDADuloxetine Delayed-Release Capsules USP, 60mg, Rx Only, 90-count bottle, Mfr. by Towa Ph…D-0522-2026
December 10, 2025FDADuloxetine Delayed-Release Capsules, USP, 60 mg, 1000-Capsule bottles, Rx Only, Manufactu…D-0215-2026
December 10, 2025FDADuloxetine Delayed-Release Capsules, USP, 60 mg, 1000-Capsule bottles, Rx Only, Manufactu…D-0216-2026
November 5, 2025FDADuloxetine Delayed-Release Capsules, USP, 60 mg, a.) 90-count bottle (NDC: 51991-748-90),…D-0100-2026
September 17, 2025FDADuloxetine Delayed-Release Capsules, USP, 30 mg, 1,000 Capsules per bottle, Rx Only, Manu…D-0621-2025
August 20, 2025FDADuloxetine Delayed-Release Capsules, USP, 60 mg, 1,000 Capsules per bottle, Rx Only, Manu…D-0580-2025
August 13, 2025FDADuloxetine Delayed-Release Capsules, USP, 60mg, 1,000-count bottles, Rx Only, Mfr. by: To…D-0552-2025
July 16, 2025FDADuloxetine Delayed-Release Capsules, USP, 40mg, 30-count bottles, Rx Only, Mfr. by: Tow…D-0511-2025
April 30, 2025FDADuloxetine Delayed-Release Capsules USP, 60 mg, 1000-count bottles, Rx Only, Manufactured…D-0387-2025
April 30, 2025FDADuloxetine Delayed-Release Capsules USP, 30 mg, a.) 90-count bottles (NDC# 51991-747-90),…D-0388-2025
April 9, 2025FDADuloxetine Delayed-Release Capsules, USP, 30 mg, Rx Only, 1,000 Capsules per bottle, Manu…D-0308-2025
March 19, 2025FDADuloxetine Delayed-Release Capsules, USP, 20mg, Rx Only, 500-count bottles, Mfr. by: Towa…D-0271-2025
March 19, 2025FDADuloxetine Delayed-Release Capsules, USP, 60mg, Rx Only, 1000-count bottles, Mfr. by: Tow…D-0269-2025
March 19, 2025FDADuloxetine Delayed-Release Capsules, USP, 30mg, Rx Only, 1000-count bottles, Mfr. by: Tow…D-0270-2025
January 1, 2025FDADuloxetine Delayed-Release Capsules, USP, 30mg, Rx Only, 90-count bottles (NDC 51991-747-…D-0161-2025
January 1, 2025FDADuloxetine Delayed-Release Capsules, USP, 60 mg, Rx Only, 90-count bottles (NDC 51991-748…D-0162-2025
October 23, 2024FDADuloxetine Delayed-Release Capsules, USP, 20mg, Rx Only, 500-count bottles, Mfr. by: Towa…D-0009-2025
June 26, 2024FDADuloxetine Delayed-Release Capsules, USP, 60mg, 90-count bottle, Rx Only, Mfr. by: Towa …D-0562-2024
May 15, 2024FDADuloxetine Delayed-Release Capsules, USP, 30mg, Rx Only, (a) 90-count bottles (NDC 51991-…D-0482-2024
May 15, 2024FDADuloxetine Delayed-Release Capsules, USP, 20 mg, , 500-count bottles, Rx Only, Mfr. by: T…D-0483-2024
May 15, 2024FDADuloxetine Delayed-Release Capsules, USP, 60 mg, 90-count bottles, Rx Only, Mfr. by: Towa…D-0484-2024
March 22, 2023FDAClobazam Tablets, 10 mg, CIV, 100-count bottle, Rx only, Manufactured by Centaur Pharmace…D-0462-2023
March 22, 2023FDAAlprazolam Tablets, USP, 2 mg, CIV, packaged in: a)100-count bottle (NDC 51991-0707-01) a…D-0461-2023

Questions about this company

How many recalls does Breckenridge Pharmaceutical, Inc have?
Recalert has 33 U.S. recalls on record for Breckenridge Pharmaceutical, Inc, published between November 18, 2015 and June 17, 2026.
What was the most recent Breckenridge Pharmaceutical, Inc recall?
FDA recall D-0583-2026, published June 17, 2026: Duloxetine Delayed-Release Capsules, USP, 60mg, packaged in a) 90 Capsules (NDC 51991-748-90); b) 1000 Capsules (51991-748-10), Rx Only, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcel…
Which agencies have handled Breckenridge Pharmaceutical, Inc recalls?
Breckenridge Pharmaceutical, Inc appears as the recalling firm in recalls from: FDA (33).

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