US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 20, 2012 (14 years ago)

Propranolol Hydrochloride Extended-release Capsules, USP, 80 mg, 100 Capsules, Rx only…

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

Why it was recalled

Failed Dissolution Test Requirements

What was recalled

Propranolol Hydrochloride Extended-release Capsules, USP, 80 mg, 100 Capsules, Rx only, Manufactured for Upsher Smith Laboratories, Inc Minneapolis MN 55447 --- NDC 0245-0085-11, UPC 3 0245-0085-11 9

Recalling firm
Upsher Smith Laboratories, Inc.
NDC code
0245-0085-11
Origin
MN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-160-2013

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.

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