US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 14, 2020 (6 years ago)

Lidocaine Patch 5%, packaged in 30-count cartons, Rx only, Manufactured by: Actavis…

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

Why it was recalled

Labeling: Incorrect or Missing Lot and/or Exp date on the individual transdermal pouches but not in the carton.

What was recalled

Lidocaine Patch 5%, packaged in 30-count cartons, Rx only, Manufactured by: Actavis Laboratories UT, Inc., Salt Lake City, UT 84108, USA, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054 USA, NDC 0591-3525-30

Recalling firm
Teva Pharmaceuticals USA
NDC code
0591-3525-30
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1492-2020

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 Lidocaine recalls

See all