Public recall detail

EVIS EXERA III Duodenovideoscope

2026-02-03

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Recall Safety notice
Quick summary

Quick summary: EVIS EXERA III Duodenovideoscope. Date: 2026-02-03.

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 Duodenovideoscope. Date: 2026-02-03.

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 Duodenovideoscope
IssueMedical devices - Labelling and packaging
Recall classType I
IdentificationRA-81566

Affected products

ProductEVIS EXERA III Duodenovideoscope
LotAll lots.
ModelTJF-Q190V
Serial numberAll lots.
DescriptionEVIS EXERA III Duodenovideoscope

Issue

Olympus has updated the reprocessing materials to minimize potential deviations in TJF duodenoscope reprocessing. Olympus is informing users of these changes and is reminding users to closely follow the operation and reprocessing instructions. Users are required to acknowledge reviewing all such materials, which can be accessed through Olympus' education portal.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Gastroenterology and urology
CompaniesOlympus Medical Systems Corp. 2951 Ishikawa-Cho, Hachioji-Shi, Tokyo-To, Japan, 192-8507
Recall date2025-10-14
Published byHealth Canada
Recall classType I
Alert / recall typeHealth product recall
Identification numberRA-81566
Background{}
CompaniesOlympus Medical Systems Corp. 2951 Ishikawa-Cho, Hachioji-Shi, Tokyo-To, Japan, 192-8507
AudiencesHealthcare
Source updated2026-02-03

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

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