HomeRecall LibraryRecall LibraryPar Health Issues Voluntary Nationwide Recall of Argatroban Injection Due to the Presence of Particulate Matter
FDA recall notice

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

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Source attribution: FDA. Published Oct 14, 2026.

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