NEW ALBANY, Ohio, Sept. 3, 2026 /PRNewswire/ -- American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received…
TOPEKA (KSNT) – Federal health officials report a company is recalling epinephrine injection vials distributed nationwide due to sterility concerns and reports of leaks in the vials. The Food and Drug Administration (FDA) announced on Sept. 3 that American Regent, Inc.
Three recalled lots may contain glass and other particles, so check the vial details before using emergency medication intended for severe allergic reactions
A U.S. drugmaker has recalled three lots of epinephrine injections after reports of leaking and cracked vials prompted concerns about product sterility, according to an alert from the Food and Drug Administration. American Regent, Inc.
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Epinephrine injection recalled over potentially fatal health risks | Since Then