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Official Product Recall

This notice was issued by U.S. Food & Drug Administration (FDA).

FDA

Par Health Issues Voluntary Nationwide Recall of Argatroban Injection Due to the Presence of Particulate Matter

FOR IMMEDIATE RELEASE - ROCHESTER, MI– October 13, 2026 – Par Health is recalling 22 lots of Argatroban Injection 250 mg/2.5 mL (100 mg/mL) to the hospital/user level. This recall is being conducted due to the presence of particulate matter, identified as cellulose, polystyrene, polyethylene terepht

This recall was published by U.S. Food & Drug Administration (FDA). View the full official notice for complete details, affected product codes, and what to do next.

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What should I do?

  • 1.Stop using the product immediately if you have it.
  • 2.Check the full recall notice for affected batch numbers, UPCs, or model numbers.
  • 3.Follow the instructions in the recall notice for returns, replacements, or disposal.
  • 4.If you have health concerns after using the product, contact your GP or call NHS 111.
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ProductSafer is not affiliated with the FDA. This page reproduces publicly available recall information.

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