Drugmaker American Regent launched a voluntary recall of epinephrine injection due to leaking and cracked multidose vials USP 30 mg/ 30 mL, 1 mg/mL.

Some epinephrine injections have been recalled, according to a new FDA notice. Here's which products are affected.

Consumers, retailers and health care facilities should stop using the product and discard or return it, the FDA said.

“Particulate matter can cause blockage and clotting in blood vessels, which can cut off blood flow to vital organs, lead to a life-threatening blood clot in the lungs (pulmonary embolism) and cause ...

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 ...

The Ohio-based company found particulate matter including glass and nylon in the vials, which can cause blood clots, organ damage, or death ...

American Regent is recalling three lots of Epinephrine Injection, USP 30 mg/30 mL (NDC 0517-3030-01) due to sterility concerns and the presence of particulate matter, including nylon, glass, acrylic, ...

American Regent, Inc. is recalling 3 lots of Epinephrine Injection, USP 30 mg/30 mL (1 mg/mL) multidose vials nationwide ...

Please provide your email address to receive an email when new articles are posted on . Epinephrine may be given via intramuscular and subcutaneous injections. Intramuscular and subcutaneous ...

LAKE ZURICH, Ill., May 20, 2025--(BUSINESS WIRE)--Fresenius Kabi, an operating company of Fresenius, announced today that Epinephrine Injection, USP, is now available in the United States in 30 mg per ...

Please provide your email address to receive an email when new articles are posted on . Recommendations for outcomes that fall between results with manual injection and autoinjectors come from the FDA ...