February 2024 FDA Recall Oseltamivir Phosphate by Amneal Pharmaceuticals Of New York, Llc
D-0327-2024 - Failed Impurities/Degradation Specifications

This Class II drug recall was voluntarily initiated by Amneal Pharmaceuticals Of New York, Llc on February 13, 2024 for the product Oseltamivir Phosphate. The FDA reported the reason for recall as failed impurities/degradation specifications. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-0327-2024

Reason for Recall
Failed Impurities/Degradation Specifications: Out-of-specification test results.
Initiated
02-13-2024
Reported
02-28-2024
Quantity
46,037 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
Amneal Pharmaceuticals of New York, LLC
Nationwide in the USA
Oseltamivir Phosphate for Oral Suspension 6mg/ml, 60 mL (reconstituted) bottle, RX only, Distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807. NDC# 69238-1273-6

Batch or Lot Expiration Information

Lot# BF22722A, Exp. 08/31/2024; BJ15122A, Exp. 09/30/2024

Affected Packages Involved in this Recall