FDA · recall · urgent
FDA: American Regent recalls Epinephrine Injection lots due to particulate matt
American Regent, Inc. voluntarily recalled three lots of Epinephrine Injection, USP 30 mg/30 mL (1 mg/mL) multi-dose vials nationwide. The recall was initiated after customer complaints of leaking and cracked vials, with concerns about particulate matter and sterility assurance.
- 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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