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

Several lots of epinephrine injection vials have been recalled over concerns about their sterility. American Regent, Inc. has ...

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

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 ...

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

“Particulate matter can cause blockage and clotting in blood vessels, which can cut off blood flow to vital organs, lead to a ...

Federal health officials report a company is recalling epinephrine injection vials distributed nationwide due to sterility ...

DifGen Pharmaceuticals LLC ("DifGen"), a US based specialty generic pharmaceutical company, today announced that the U.S. Food and Drug Administration (FDA) approved its Abbreviated New Drug ...

The U.S. Food & Drug Administration (FDA) is warning the public that some vials of Tyenne have been recalled. The affected vials are being recalled over concerns they may contain glass particles. Here ...

Endo’s Par Sterile Products business has begun shipping bivalirudin injection in a ready-to-use 250 mg/50 ml single-use vial. It is the only ready-to-use liquid format of bivalirudin on the market in ...