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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.

Read the notice at fda.gov →

Agency
FDA
Jurisdiction
US-FDA
Action type
recall
Severity
urgent — penalty-bearing, effective immediately, or a serious health hazard
Published
Recorded
Tags
recallepinephrineinjectableparticulate-mattersterility
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