Reported Aug 19, 2020 · Terminated

Lidocaine Patch 5%, packaged in 30-count cartons, Rx only, Manufactured by: Actavis Laboratories UT, Inc., Salt Lake…

Teva Pharmaceuticals USA

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Teva Pharmaceuticals USA · 400 Interpace Pkwy · Parsippany, NJ · 07054-1120

Is this the product you have?

    • Lidocaine Patch 5%
    • packaged in 30-count cartons
    • Rx only
  • Manufactured byActavis Laboratories UT, Inc., Salt Lake City, UT 84108, USA
  • Distributed byActavis Pharma, Inc., Parsippany, NJ 07054 USA, NDC 0591-3525-30
Lot codes and dates
    • Carton Lot # 1383513B
    • Patch Lot # 1383513
    • Exp date 03/2022
Amount recalled
28,596 cartons

Where it was sold

  • Nationwide

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Jul 7, 2021 · Data as of Sep 19, 6:36 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.