PlainRecalls
FDA Drug Low Class III Terminated

METHOCARBAMOL TABLETS, USP 500 mg, 500 Count Bottles, Rx Only. Manufactured by AustarPharma LLC, Edison, NJ 08837, USA, Packaged by GSMS Incorporated, Camarillo, CA 93012, USA, NDC: 60429-118-05.

Reported: September 16, 2015 Initiated: August 11, 2015 #D-1426-2015

Product Description

METHOCARBAMOL TABLETS, USP 500 mg, 500 Count Bottles, Rx Only. Manufactured by AustarPharma LLC, Edison, NJ 08837, USA, Packaged by GSMS Incorporated, Camarillo, CA 93012, USA, NDC: 60429-118-05.

Reason for Recall

Presence of Foreign Substance: Presence of hair.

Details

Units Affected
1,165 Bottles
Distribution
U.S. Including: GA.
Location
Camarillo, CA

Frequently Asked Questions

What product was recalled?
METHOCARBAMOL TABLETS, USP 500 mg, 500 Count Bottles, Rx Only. Manufactured by AustarPharma LLC, Edison, NJ 08837, USA, Packaged by GSMS Incorporated, Camarillo, CA 93012, USA, NDC: 60429-118-05.. Recalled by Golden State Medical Supply Inc.. Units affected: 1,165 Bottles.
Why was this product recalled?
Presence of Foreign Substance: Presence of hair.
Which agency issued this recall?
This recall was issued by the FDA Drug on September 16, 2015. Severity: Low. Recall number: D-1426-2015.