Drugmaker American Regent launched a voluntary recall of epinephrine injection due to leaking and cracked multidose vials USP ...

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

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

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 ...

A drug manufacturer has issued a recall epinephrine injections after complaints the vials were cracked or leaking and ...

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 ...

American Regent is recalling three lots of Epinephrine Injection, USP 30 mg/30 mL (NDC 0517-3030-01) due to sterility ...

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 ...

An adrenaline auto-injector is an emergency treatment for anaphylaxis; serious and potentially fatal allergic reaction to insect stings, medicines, or food, among others. Anaphylaxis is an ...

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