PlainRecalls
FDA Drug Low Class III Terminated

TRAMADOL HYDROCHLORIDE Tablets, USP, 50 mg, Rx Only a)100-count bottles (NDC 60429-588-01) b) 500-count bottle (NDC 60429-588-05) Manufactured by Teva Czech Industries, s.r.o. Opava-Komarov, Czech Republic, Packaged by GSMS Incorporated, Camarillo, CA 93012

Reported: March 4, 2020 Initiated: February 12, 2020 #D-0856-2020

Product Description

TRAMADOL HYDROCHLORIDE Tablets, USP, 50 mg, Rx Only a)100-count bottles (NDC 60429-588-01) b) 500-count bottle (NDC 60429-588-05) Manufactured by Teva Czech Industries, s.r.o. Opava-Komarov, Czech Republic, Packaged by GSMS Incorporated, Camarillo, CA 93012

Reason for Recall

Labeling: Incorrect package insert - Patient leaflets for the specified lots of unscored tablets contain language relative to a 25 mg dosing titration that necessitates the use of a scored 50 mg tablet.

Details

Units Affected
379,043 100-ct bottles and 330,997 500-ct bottles
Distribution
Distributed Nationwide in the USA
Location
Camarillo, CA

Frequently Asked Questions

What product was recalled?
TRAMADOL HYDROCHLORIDE Tablets, USP, 50 mg, Rx Only a)100-count bottles (NDC 60429-588-01) b) 500-count bottle (NDC 60429-588-05) Manufactured by Teva Czech Industries, s.r.o. Opava-Komarov, Czech Republic, Packaged by GSMS Incorporated, Camarillo, CA 93012. Recalled by Golden State Medical Supply Inc.. Units affected: 379,043 100-ct bottles and 330,997 500-ct bottles.
Why was this product recalled?
Labeling: Incorrect package insert - Patient leaflets for the specified lots of unscored tablets contain language relative to a 25 mg dosing titration that necessitates the use of a scored 50 mg tablet.
Which agency issued this recall?
This recall was issued by the FDA Drug on March 4, 2020. Severity: Low. Recall number: D-0856-2020.