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Life-saving medicine recalled after reports of contamination

Product Recall

Published: 18:36 EDT, 7 September 2026 | Updated: 18:36 EDT, 7 September 2026 A medication used for the emergency treatment of a life-threatening allergic reaction is being recalled over concerns of sterility and the possible presence of particulate matter.

Cases and health response

Ohio-based American Regent Inc. is conducting a nationwide recall of three lots of its Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials.

Epinephrine is used to emergently treat life-threatening allergic reactions, such as anaphylaxis, which can be caused by insect stings, foods or medications.

It can also be used to increase blood pressure in critically ill patients suffering from life-threatening septic shock.

The recall was initiated after the company received complaints from consumers detailing leaking and cracked vials, which resulted in the lack of assurance of sterility.

The FDA warns that intravenous administration of an epinephrine injection containing particulate matter could lead to 'serious adverse health consequences.'

Health investigation

An investigation then revealed the presence of particulate matter identified as nylon, cellulose, acrylic, polyethylene and glass.

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