FDA recall record

Ciprofloxacin Tablets USP, 500 mg, 100-count bottle recall — FDA D-220-2013

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

Class IIclassification
D-220-2013official record ID
Apr 3, 2013report date

Recall record at a glance

Official recordD-220-2013
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmWest-ward Pharmaceutical Corp.
Report dateApr 3, 2013
Recall initiation dateFeb 6, 2013
Quantity7,136 units
LocationEatontown, NJ, United States

Official product description

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

Why the product was recalled

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

Distribution information

GA, AR

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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