Anticoagulant recalled over life-threatening risk
MDSpire News
October 15, 2026
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Par Health USA voluntarily recalled 22 lots of argatroban injection nationwide after detecting particulate contamination.
The particles included cellulose, polystyrene, polyethylene terephthalate, stopper material, and possibly stainless steel.
The company warned that affected injections could cause pulmonary emboli, vascular occlusion with tissue or organ damage, and venous inflammation that may lead to clot formation.
The recall covers 20 lots under NDC 42023-182-01 and 2 lots under NDC 42023-182-89, distributed to US wholesalers and hospitals from December 30, 2024, through May 5, 2026.
Wholesale distributors and hospital pharmacies should immediately stop using and distributing affected lots, and notify downstream recipients if products were redistributed.
This content is an AI-generated, fully rewritten summary based on a published scholarly article. It does not reproduce the original text and is not a substitute for the original publication. Readers are encouraged to consult the source for full context, data, and methodology.
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