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Class I · Most seriousActive recall

Argatroban

A reasonable chance it could cause serious harm or death.

Does this affect you?
Check your lot numberLot #: 84193, Exp Date: 10/2026; 92880, Exp Date: 08/2027.
Where it was soldNationwide within the United States
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

Particulate matter: particulate matter identified as cellulose, polystyrene, polyethylene teraphalate, stainless steel, or stopper material in the product solution.

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 byPar Health USA, LLC
Brand nameARGATROBAN
Generic nameARGATROBAN
Active ingredient(s)ARGATROBAN
Distributed by / forPar Pharmaceutical, Cranbury, NJ 08512
NDC42023-182-89
Show the full FDA record
Full product labelArgatroban Injection, USP, 250 mg/2.5mL (100 mg/mL), 2.5 mL x 1 Single Dose Vial, Rx only, Manufactured for: Endo USA, Malvern,PA 19355/ Argatroban Injection, 250 mg/2.5mL (100 mg/mL), 2.5 mL x 1 Single Dose Vial, Rx only, Distributed by: Par Pharmaceutical, Cranbury, NJ 08512, NDC 42023-182-89.
Recalling firmPar Health USA, LLC
DistributionNationwide within the United States
Quantity1944 vials
Recall initiated2026-10-13
Report date2026-10-28
Recall completed—
Recall numberD-0083-2027
ClassificationClass I
FDA statusOngoing
Origin on fileRochester MI United States

Related

Recent drug recallsCheck another medication

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.