US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 22, 2014 (12 years ago)

Ciprofloxacin 500 mg tablets, 20 count bottle, Rx only, Packaged by Aidarex…

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

Why it was recalled

Presence of Foreign Tablets/Capsules: Tramodol 50 mg tablet has been found in a bottle of Ciprofloxacin 500 mg

What was recalled

Ciprofloxacin 500 mg tablets, 20 count bottle, Rx only, Packaged by Aidarex Pharmacecuticals LLC, MFG: Unique Pharmaceutical Laboratories, Mumbai, India

Recalling firm
Aidarex Pharmaceuticals LLC
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0042-2015

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.

Other Ciprofloxacin recalls

See all