US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 13, 2022 (4 years ago)

Lidocaine Patch 5%, 30-count carton, Rx only, MFG: Qualitest Products, NDC 0603-1880-16

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

Why it was recalled

cGMP deviations: Temperature abuse

What was recalled

Lidocaine Patch 5%, 30-count carton, Rx only, MFG: Qualitest Products, NDC 0603-1880-16

Recalling firm
Mckesson Medical-Surgical Inc. Corporate Office
NDC code
0603-1880-16
Origin
VA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1043-2022

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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