Class II
Ongoing
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
This recall is currently active, issued January 24, 2024. It was issued by Ascend Laboratories, Llc.
- Company
- Ascend Laboratories, Llc
- Recall Initiated
- December 29, 2023
- Posted
- January 24, 2024
- Recall Number
- D-0237-2024
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 3,288 bottles
- Firm Location
- Parsippany, NJ, United States
- Official Source
- View on FDA website ↗
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.
Distribution
Nationwide
Lot / Code Info
23140190, Exp. Date 12/31/2024
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