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FDAJanuary 4, 2021device

INJECTOR FORCEMAX UP 2MM CH 23G 6MM, model no. NM-401L-0623 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

What to do

FDA enforcement status: Terminated

Brands named

aomori olympusaomori

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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