Reported Jan 24, 2024 · Ongoing
Ibuprofen and Famotidine Tablets 800mg/26.6mg, Rx Only, 90 Tablets per Bottle, manufactured by: Alkem Laboratories…
Ascend Laboratories, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Ascend Laboratories, LLC · 339 Jefferson Rd Ste 101 · Parsippany, NJ · 07054-3707
Is this the product you have?
- Ibuprofen and Famotidine Tablets 800mg/26.6mg, Rx Only, 90 Tablets per Bottle
- manufactured byAlkem Laboratories Ltd., INDIA
- Distributed byAscend Laboratories, LLC., Parsippany, NJ 07054, NDC 67877-626-90
- Lot codes and dates
23140190Exp. Date 12/31/2024
- Amount recalled
- 3,288 bottles
Where it was sold
- Nationwide
Why it was recalled
Presence of Foreign Tablet/Capsule: A stray Rasagiline Mesylate 1 mg tablet was discovered in an unopened bottle of Ibuprofen and Famotidine.
This product could cause temporary or reversible health problems — stop using it.
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