December 2023 FDA Recall Ibuprofen And Famotidine by Ascend Laboratories, Llc
D-0237-2024 - Presence of Foreign Tablet/Capsule

This Class II drug recall was voluntarily initiated by Ascend Laboratories, Llc on December 29, 2023 for the product Ibuprofen And Famotidine. The FDA reported the reason for recall as presence of foreign tablet/capsule. The product was distributed Nationwide and the recall is currently ongoing.

Recall Number: D-0237-2024

Reason for Recall
Presence of Foreign Tablet/Capsule: A stray Rasagiline Mesylate 1 mg tablet was discovered in an unopened bottle of Ibuprofen and Famotidine.
Initiated
12-29-2023
Reported
01-24-2024
Quantity
3,288 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
Ascend Laboratories, LLC
Ibuprofen and Famotidine Tablets 800mg/26.6mg, Rx Only, 90 Tablets per Bottle, manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories, LLC., Parsippany, NJ 07054, NDC 67877-626-90

Batch or Lot Expiration Information

Lot# 23140190, Exp. Date 12/31/2024