Public recall detail

HD ENDOEYE™ Laparo-Thoraco Videoscope

2023-12-06

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Recall Safety notice
Quick summary

Quick summary: HD ENDOEYE™ Laparo-Thoraco Videoscope. Date: 2023-12-06.

Recommended action

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

Recall details

Quick summary: HD ENDOEYE™ Laparo-Thoraco Videoscope. Date: 2023-12-06.

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.
ProductHD ENDOEYE™ Laparo-Thoraco Videoscope
IssueMedical devices - Labelling and packaging
Recall classType II
IdentificationRA-74708

Affected products

ProductHD ENDOEYE™ Laparo-Thoraco Videoscope
LotMore than 10 numbers, contact manufacturer.
ModelLTF-S190-10 LTF-S190-5
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionHD ENDOEYE™ Laparo-Thoraco Videoscope

Issue

During an evaluation of user implementation of the instructions for use related to the reprocessing of the LTF-S190-5 videoscope, Olympus observed deviations from the following reprocessing steps detailed in the respective reprocessing manual instructions. Recall start date: November 23, 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-74708
Background{}
CompaniesOlympus Medical Systems Corp. 2951 Ishikawa-Cho, Hachioji-Shi, Tokyo-To, Japan, 192-8507
AudiencesHealthcare
Source updated2023-12-06

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

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