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Class II · ModerateRecall completed

Oseltamivir Phosphate

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot # BF22722A, Exp. 08/31/2024; BJ15122A, Exp. 09/30/2024
Where it was soldNationwide in the USA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Failed Impurities/Degradation Specifications: Out-of-specification test results.

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byAmneal Pharmaceuticals NY LLC
Brand nameOSELTAMIVIR PHOSPHATE
Generic nameOSELTAMIVIR PHOSPHATE
Active ingredient(s)OSELTAMIVIR PHOSPHATE
Distributed by / forAmneal Pharmaceuticals LLC, Bridgewater, NJ 08807
NDC69238-1273-6
Show the full FDA record
Full product labelOseltamivir Phosphate for Oral Suspension 6mg/ml, 60 mL (reconstituted) bottle, RX only, Distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807. NDC# 69238-1273-6
Recalling firmAmneal Pharmaceuticals of New York, LLC
DistributionNationwide in the USA
Quantity46,037 Bottles
Recall initiated2024-02-13
Report date2024-02-28
Recall completed2025-02-14
Recall numberD-0327-2024
ClassificationClass II
FDA statusTerminated
Origin on fileBrookhaven NY United States

Related

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Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.