Health product recall

Duodenoscope (2020-04-30)

Starting date:
April 30, 2020
Posting date:
May 29, 2020
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-73207



Last updated: 2020-05-29

Affected Products

Duodenoscope

Reason

The detachment of the disposable DC-07D distal end cap from the ED-580XT duodenoscope during patient procedures.

Affected products

Duodenoscope

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number

ED-580XT

Companies
Manufacturer

Fujifilm Corporation

26-30 NISHIAZABU, 2 CHOME MINATO-KU

TOKYO-TO

JAPAN