Reported Sep 2, 2020 · Terminated

Losartan Potassium Tablets USP, 50 mg, 90 count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc.,…

Hetero Labs Limited (Unit V)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Hetero Labs Limited (Unit V) · 458 Surv No 439 - 441 · Badepalle, N/A · N/A

Is this the product you have?

  • Losartan Potassium Tablets USP, 50 mg, 90 count bottles, Rx only
  • Manufactured forCamber Pharmaceuticals, Inc., Piscataway, NJ by Hetero Labs, Limited, Mahabubragar, India
Lot codes and dates
    • Batch # LOA19357A
    • exp. date 09/2021
Amount recalled
43,512 bottles

Why it was recalled

Failed Tablet/Capsule Specification; complaint of bulging tablet

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Jan 24, 2022 · Data as of Sep 19, 7:58 PM UTC

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