RecallRadar

FDA Drug recall D-189-2013

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…

On 2013-03-13 the FDA classified a Class II recall of 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… by West Ward Pharmaceutical, citing discoloration: Ethambutol Tablets USP 400 mg have tablets cores that may be discolored.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-189-2013
ClassificationClass II
Statusterminated
Initiated2012-11-30
Published2013-03-13
Last updated2026-09-13 11:51 UTC
CompanyWest Ward Pharmaceutical
DistributionGA

Product

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

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

Identifiers

code_info68977A; 68977B; 68978B; 68978C; 68979A - exp JUL 2015 68977C; 68978A exp JUL 2013

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-189-2013%22

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