US Drug Recall Register
Class III · Low risk Terminated Initiated Feb 15, 2023 (4 years ago)

Buprenorphine Transdermal System, CIII 10 mcg/hour, 4 Transdermal Systems One package of…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Impurities/Degradation Specifications: Out of specification for related substance 10-hydroxy buprenorphine N-Oxide results generated at the 18-month stability timepoint.

What was recalled

Buprenorphine Transdermal System, CIII 10 mcg/hour, 4 Transdermal Systems One package of 4 disposal units, Rx Only, Manufactured by: Aveva Drug Delivery Systems Inc. Miramar, FL. 33025, Manufactured for: Apotex Corp Weston, FL. 33326, NDC 60505-7077-05

Recalling firm
AVEVA Drug Delivery Systems, Inc.
NDC code
60505-7077-05
Origin
FL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0465-2023

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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