Recall Atlas
Drugs & medicalClass I

Par Health USA, LLC recalls Argatroban 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…

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

Read the official notice →
Date
2026-10-28
Country
United States
Brand
Par Health
Product
Argatroban 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…
Classification
Class I
Units
Nationwide within the United States
Category
Drugs & medical
Source
FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Par Health recalls

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    Crystallization; identified as Buprenorphine free base

    FDA · DrugPar Health USA, LLCNationwide in the USA.Official notice →
All 3 Par Health recalls →

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    FDA · DrugHikma Pharmaceuticals USA INC.Nationwide within the United StatesOfficial notice →
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