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Class II: temporary or reversible health riskTerminated

Avkare Losartan Potassium Tablets 50 mg 50 Tablets Recall

Losartan Potassium Tablets USP 50 mg 50 Tablets (5x10) Unit Dose boxes, Rx Only, Manufa…

AVKARE Inc. · Pulaski, TN

Risk level
Class II
Reported by FDA
Mar 27, 2019
Recall ID
D-1044-2019
Check your lot numberHow we source this data

Summary

Avkare recalled Losartan Potassium Tablets 50 mg 50 Tablets starting Mar 5, 2019. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1044-2019 on Mar 27, 2019. Reason: CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) was identified. Status: Terminated.

Why it was recalled

CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) was identified

Product description

Losartan Potassium Tablets USP 50 mg 50 Tablets (5x10) Unit Dose boxes, Rx Only, Manufactured for: AvKARE Inc. Pulaski, TN 38478 ---- NDC 50268-517-15

Lot numbers, UPCs & expiration codes

Lots: 20961 Exp. 09/2019; 20477 Exp. 08/2019

Where it was sold

Nationwide.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1044-2019
Classification
Class II
Status
Terminated
Recall initiated
Mar 5, 2019
FDA report date
Mar 27, 2019
Quantity
N/A
Recall type
Voluntary: Firm initiated
Recalling firm
AVKARE Inc.

Original FDA data

Every field from FDA enforcement report D-1044-2019, exactly as published.

Show all FDA fields
City
Pulaski
State
TN
Status
Terminated
Country
United States
Event ID
82314
Address
615 N 1st St
Code information
Lots: 20961 Exp. 09/2019; 20477 Exp. 08/2019
Postal code
38478-2403
Report date
Mar 27, 2019
Product type
Drugs
Recall number
D-1044-2019
Classification
Class II
Recalling firm
AVKARE Inc.
Termination date
Dec 7, 2020
Reason for recall
CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) was identified
Voluntary / mandated
Voluntary: Firm initiated
Product description
Losartan Potassium Tablets USP 50 mg 50 Tablets (5x10) Unit Dose boxes, Rx Only, Manufactured for: AvKARE Inc. Pulaski, TN 38478 ---- NDC 50268-517-15
Distribution pattern
Nationwide.
Recall initiation date
Mar 5, 2019
Initial firm notification
Letter
Center classification date
Mar 21, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1044-2019, published Mar 27, 2019. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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