FDA recall D-1492-2020

Teva Pharmaceuticals USA · Class II · drug

Product

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

Reason for recall

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

Distribution

Nationwide United States

Key facts

Status
Terminated
Initiation date
2020-07-14
Report date
2020-08-19
Termination date
2021-07-07
Voluntary/Mandated
Voluntary: Firm initiated
Location
Parsippany, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1492-2020