US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jan 23, 2013 (14 years ago)

Terazosin Hydrochloride Capsules, 2 mg, packaged in a) 100-count bottles (NDC…

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

Why it was recalled

Presence of Foreign Tablets/Capsules: Recall is being conducted due to a foreign capsule found in one bottle.

What was recalled

Terazosin Hydrochloride Capsules, 2 mg, packaged in a) 100-count bottles (NDC 0093-4337-01); and b) 1000-count bottles (NDC 0093-4337-10), Rx only, Manufactured in India By: Intas Pharmaceuticals Ltd., Ahmedabad, Gujarat, India - 382 210; Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA 18960.

Recalling firm
Teva Pharmaceuticals USA, Inc.
NDC code
0093-4337-01
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-193-2013

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 Chloride recalls

See all