FDA recall record

Metoprolol Tartrate Tablets USP 100 mg, 1000-count bottles recall — FDA D-0812-2021

Presence of Foreign Substance: Product complaints received for the presence of metal wire in one tablet.

Class IIclassification
D-0812-2021official record ID
Sep 29, 2021report date

Recall record at a glance

Official recordD-0812-2021
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAurobindo Pharma USA Inc.
Report dateSep 29, 2021
Recall initiation dateSep 9, 2021
Quantity2,820 bottles
LocationEast Windsor, NJ, United States

Official product description

Metoprolol Tartrate Tablets USP 100 mg, 1000-count bottles, Rx only, Distributed by: Aurobindo Pharma USA Inc. 279 Princeton-Highstown Road East Windsor, NJ 08520, NDC 65862-064-99

Why the product was recalled

Presence of Foreign Substance: Product complaints received for the presence of metal wire in one tablet.

Distribution information

Nationwide within the United States

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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