March 2025 FDA Recall Duloxetine by Breckenridge Pharmaceutical, Inc.
D-0308-2025 - CGMP Deviations

This Class II drug recall was voluntarily initiated by Breckenridge Pharmaceutical, Inc. on March 26, 2025 for the product Duloxetine. The FDA reported the reason for recall as cgmp deviations. The product was distributed Nationwide and the recall is currently ongoing.

Recall Number: D-0308-2025

Reason for Recall
CGMP Deviations: presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the recommended interim limit.
Initiated
03-26-2025
Reported
04-09-2025
Quantity
14,863 bottles

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Breckenridge Pharmaceutical, Inc.
Nationwide in the US
Duloxetine Delayed-Release Capsules, USP, 30 mg, Rx Only, 1,000 Capsules per bottle, Manufactured by: Towa Pharmaceutical Europe, S.L., Martorelles, (Barcelona), Spain, Distributed by: Breckenridge Pharmaceutical, Inc., Berkley Heights, NJ 07922, NDC 51991-747-10.

Batch or Lot Expiration Information

Lot# Lot 240909C, Exp Date 03/31/2027