FDA · recall · urgent
FDA: Par Health recalls Argatroban Injection due to particulate matter
Par Health is recalling 22 lots of Argatroban Injection 250 mg/2.5 mL (100 mg/mL) to the hospital/user level due to the presence of particulate matter, identified as cellulose, polystyrene, and polyethylene terephthalate.
- Agency
- FDA
- Jurisdiction
- US-FDA
- Action type
- recall
- Severity
- urgent — penalty-bearing, effective immediately, or a serious health hazard
- Published
- Recorded
- Tags
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