The Recall Desk
SevereFDA (Drugs)·D-1250-2019·Announced 2019-05-08

AvKARE Recalls Losartan Potassium Tablets Due to Impurity

AvKARE Inc. is recalling Losartan Potassium Tablets 25 mg because FDA testing found an impurity above acceptable levels.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall is classified as FDA Class II, and the presence of a nitrosamine impurity (NMBA) above acceptable limits represents a significant health risk, aligning with the 'Severe' criteria for significant injury/property-damage reports or high-risk contamination.

Plain-English summary

AvKARE Inc. is recalling Losartan Potassium Tablets USP 25 mg (NDC 50268-516-15). The recall involves 846 cartons containing 42,300 tablets, distributed nationwide. The specific lot number is 19554, with an expiration date of 4/30/2019.

The recall was initiated due to Current Good Manufacturing Practice (CGMP) deviations. FDA laboratory testing confirmed the presence of the impurity N-Methylnitrosobutyric acid (NMBA) in the finished product at levels exceeding the interim acceptable daily intake limit of 0.96 parts per million.

Consumers and healthcare providers should check their inventory for this specific lot and expiration date. If found, the product should be discontinued and returned to the supplier or disposed of according to local regulations.

The recalled product

Product
Losartan Potassium Tablets USP 25 mg 50 tablets (5x10) Unit Dose Rx Only NDC 50268-516-15 Manufactured for: AvKARE Inc. Pulaski, TN 38478
Manufacturer
AVKARE Inc.
Category
Drug — Prescription Medication
Hazard

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot: 19554 Exp. 4/30/2019

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 2 recalled by AVKARE Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 2 products in this recall →

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