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.

FDA recall notice · announced September 16, 2015 · Golden State Medical Supply

Class III FDA/FSIS Class III: use is not likely to cause adverse health consequences.

The product

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.

Notes

Distribution: U.S. Including: GA.
Lot/code information: Lot # GS007849, Expiry: 02/2017
Quantity: 1,165 Bottles
Status: Terminated
Products in this recall event:
- 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. (D-1426-2015)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.