PlainRecalls
FDA Drug Moderate Class II Terminated

VERSAPHARM Ethambutol Tablets, USP,400 mg, Rx Only a)60 tablets, NDC 61748-014-06, b)90 tablets, NDC 61748-014-09, c)100 tablets, NDC 61748-014-01, d)1000 tablets, NDC 61748-014-10, e) blister pack (10s) 61748-014-11 Manufactured for: VersaPharm Incorporated Marietta, GA 30062-2260, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724.

Reported: March 13, 2013 Initiated: November 30, 2012 #D-189-2013

Product Description

VERSAPHARM Ethambutol Tablets, USP,400 mg, Rx Only a)60 tablets, NDC 61748-014-06, b)90 tablets, NDC 61748-014-09, c)100 tablets, NDC 61748-014-01, d)1000 tablets, NDC 61748-014-10, e) blister pack (10s) 61748-014-11 Manufactured for: VersaPharm Incorporated Marietta, GA 30062-2260, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724.

Reason for Recall

Discoloration: Ethambutol Tablets USP 400 mg have tablets cores that may be discolored.

Details

Units Affected
18,825 bottles
Distribution
GA
Location
Eatontown, NJ

Frequently Asked Questions

What product was recalled?
VERSAPHARM Ethambutol Tablets, USP,400 mg, Rx Only a)60 tablets, NDC 61748-014-06, b)90 tablets, NDC 61748-014-09, c)100 tablets, NDC 61748-014-01, d)1000 tablets, NDC 61748-014-10, e) blister pack (10s) 61748-014-11 Manufactured for: VersaPharm Incorporated Marietta, GA 30062-2260, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724.. Recalled by West-ward Pharmaceutical Corp.. Units affected: 18,825 bottles.
Why was this product recalled?
Discoloration: Ethambutol Tablets USP 400 mg have tablets cores that may be discolored.
Which agency issued this recall?
This recall was issued by the FDA Drug on March 13, 2013. Severity: Moderate. Recall number: D-189-2013.