FDA recall record

West-Ward Pharmaceutical Carisoprodol Tablets, USP 350 mg recall — FDA D-367-2014

Presence of Foreign Substance; heavy metals (chromium, titanium etc) and inactive components of the product were visually observed during routine…

Class IIclassification
D-367-2014official record ID
Dec 25, 2013report date

Recall record at a glance

Official recordD-367-2014
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmWest-Ward Pharmaceutical Corp.
Report dateDec 25, 2013
Recall initiation dateNov 7, 2013
Quantity20,534 bottles
LocationEatontown, NJ, United States

Official product description

Carisoprodol Tablets, USP 350 mg, Rx Only, 1000 tablets. Dist by: West-ward Pharmaceutical Corp. Eatontown, NJ 07724. Mfd by: Shasun Chemicals and Drugs Limited, Unit II, R. S. Na 32, 33, 743 PIMS Rd, Periyakalepet, Pondicherry. 605014 INDIA. NDC 0143-9749-10.

Why the product was recalled

Presence of Foreign Substance; heavy metals (chromium, titanium etc) and inactive components of the product were visually observed during routine stability testing

Distribution information

Nationwide

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

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