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Aomori Olympus Co., Ltd. recalls CRESCENT SNARE, model no. SD-221L-25 - Product Usage: Used with endoscopes to electrosurgically resect tissue within the

Recalled February 17, 2021 · FDA recall Z-1070-2021 · Aomori Olympus

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. · FDA Class II
Units
7,400,000 (globally); 260,395 (US)
Sold at
US Nationwide distribution.

Description

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.

Product
CRESCENT SNARE, model no. SD-221L-25 - Product Usage: Used with endoscopes to electrosurgically resect tissue within the digestive tract.
Manufacturer(s)
Aomori Olympus Co., Ltd.
Made in
Japan

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Aomori Olympus Co., Ltd. recalls CRESCENT SNARE, model no. SD-221L-25 - Product Usage: Used with endoscopes to electrosurgically resect tissue within the | RecallWatchUSA