RecallRadar

FDA Drug recall D-220-2013

Ciprofloxacin Tablets USP, 500 mg, 100-count bottle, Rx only, Manufactured for West-ward Pharmaceutical Corp., Eatowntown, NJ 07724 by Hikm…

On 2013-04-03 the FDA classified a Class II recall of Ciprofloxacin Tablets USP, 500 mg, 100-count bottle, Rx only, Manufactured for West-ward Pharmaceutical Corp., Eatowntown, NJ 07724 by Hikm… by West Ward Pharmaceutical, citing presence of Foreign Substance(s): A complaint was received for a rubber-like material in a 500 mg Ciprofloxacin tablet.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-220-2013
ClassificationClass II
Statusterminated
Initiated2013-02-06
Published2013-04-03
Last updated2026-09-13 11:51 UTC
CompanyWest Ward Pharmaceutical
DistributionAR, GA

Product

Ciprofloxacin Tablets USP, 500 mg, 100-count bottle, Rx only, Manufactured for West-ward Pharmaceutical Corp., Eatowntown, NJ 07724 by Hikma Pharmaceuticals, Amman, Jordan, NDC 0143-9928-01

Reason

Presence of Foreign Substance(s): A complaint was received for a rubber-like material in a 500 mg Ciprofloxacin tablet.

Identifiers

ndc0143-9927-01
ndc0143-9927-05
ndc0143-9927-30
ndc0143-9928-01
ndc0143-9928-05
ndc0143-9928-30
ndc0143-9929-01
ndc0143-9929-50
code_infoLot #: CB222A, Exp 06/16

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-220-2013%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.