Public recall detail

Evis Exera III Video System - Gastrointestinal Videoscope

2023-11-01

medium
Recall Safety notice
Quick summary

Quick summary: Evis Exera III Video System - Gastrointestinal Videoscope. Date: 2023-11-01.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Evis Exera III Video System - Gastrointestinal Videoscope. Date: 2023-11-01.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandOLYMPUS MEDICAL SYSTEMS CORP.
ProductEvis Exera III Video System - Gastrointestinal Videoscope
IssueMedical devices - Sterility
Recall classType II
IdentificationRA-74508

Affected products

ProductEvis Exera III Video System - Gastrointestinal Videoscope
LotAll lots
ModelGIF-1TH190
Serial numberAll lots
DescriptionEvis Exera III Video System - Gastrointestinal Videoscope

Issue

The GIF-1TH190 reprocessing manual has instructions for either High Level Disinfection (HLD) reprocessing or Ethylene Oxide Gas (EOG) sterilization after endoscope cleaning. As a result of testing, Olympus discovered EOG sterilization failures in which the GIF-1TH190 failed to achieve sterilization following the GIF-1TH190's reprocessing manual. As a result of the subsequent investigation, Olympus determined that changes are required to the endoscope's channel drying steps following cleaning and prior to EOG sterilization in order to ensure effective endoscope sterilization. Accordingly, Olympus has updated the instructions for the endoscope channel's drying process and validated that the new, updated channel drying steps will result in GIF-1TH190 endoscope EOG sterilization. The revised instructions for the "dry the endoscope" in chapter 5.7 of the GIF-1TH190 reprocessing manual are provided in a supplied addendum. Recall start date: October 11, 2023

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - General and plastic surgery
CompaniesOlympus Medical Systems Corp. 2951 Ishikawa-Cho, Hachioji-Shi, Tokyo-To, Japan, 192-8507
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-74508
Background{}
CompaniesOlympus Medical Systems Corp. 2951 Ishikawa-Cho, Hachioji-Shi, Tokyo-To, Japan, 192-8507
AudiencesHealthcare
Source updated2023-11-01

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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