FDA recall record

Mylan Pharmaceuticals Lisinopril Tablets, USP 10 mg recall — FDA D-269-2013

Tablets/Capsules Imprinted With Wrong ID: Pharmaceuticals are imprinted with an incorrect identifier code on the embossed tablets..

Class IIIclassification
D-269-2013official record ID
May 1, 2013report date

Recall record at a glance

Official recordD-269-2013
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmMylan Pharmaceuticals Inc.
Report dateMay 1, 2013
Recall initiation dateFeb 26, 2013
Quantity2,405 bottles
LocationMorgantown, WV, United States

Official product description

Lisinopril Tablets, USP 10 mg, Rx only, 1000 count bottles, Manufactured for: Mylan Pharmaceuticals Inc ,Morgantown, WV 26505 U.S.A. Made in India; NDC 0378-20740-10

Why the product was recalled

Tablets/Capsules Imprinted With Wrong ID: Pharmaceuticals are imprinted with an incorrect identifier code on the embossed tablets..

Distribution information

Nationwide.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement 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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