FDA recall record

Benazepril HCl Tablets, USP 40 mg, 100 count bottles recall — FDA D-0134-2020

Presence of Foreign Tablet/Capsule; Promethazine HCl tablet found in the Benazepril HCl bottle

Class IIIclassification
D-0134-2020official record ID
Oct 16, 2019report date

Recall record at a glance

Official recordD-0134-2020
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmAmneal Pharmaceuticals, Inc.
Report dateOct 16, 2019
Recall initiation dateSep 24, 2019
Quantity9,720 100 count bottles
LocationBrookhaven, NY, United States

Official product description

Benazepril HCl Tablets, USP 40 mg, 100 count bottles, Rx only, Distributed by Amneal Pharmaceuticals, Bridgewater, NJ NDC 65162-754-10

Why the product was recalled

Presence of Foreign Tablet/Capsule; Promethazine HCl tablet found in the Benazepril HCl bottle

Distribution information

Product was distributed to 13 major distributors throughout the United States who may have further distribute the product.

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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