US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jan 22, 2021 (6 years ago)

Cephalexin for Oral Suspension, USP 250 mg per 5 mL 200 ml (when mixed) Rx Only…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations: Individual Unidentified impurities results of the product was found at higher side of the specification limit.

What was recalled

Cephalexin for Oral Suspension, USP 250 mg per 5 mL 200 ml (when mixed) Rx Only, Manufactured by: Alkem Laboratories, Ltd, Mumbai -400 013 INDIA Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054 NDC 67877-545-68

Recalling firm
Ascend Laboratories LLC
NDC code
67877-545-68
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0264-2021

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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