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.

The FDA accepted an investigational new drug application for the epinephrine intranasal powder OX640 for treating anaphylaxis ...

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

“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 ...

Medical technology company Sempresto, developing a smartphone-integrated drug delivery platform designed to make rescue medications more readily available when needed, today announced a positive ...

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.

Consumers using the potentially contaminated injections could suffer adverse health consequences, the FDA warned.

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, 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 ...

Food Allergy Canada says Alberta is the only province that legislates all schools to stock epinephrine devices that aren't ...