Health Products

Single Use Guide Sheath Kit

· Published by Health Canada · Official notice

Details

Alert type: Health product recall
Category: Health products - Medical devices - Gastroenterology and urology
Product: Single Use Guide Sheath Kit
Issue: Medical devices - Performance
What to do: Contact the manufacturer if you require additional information.
Audience: Healthcare
Recall class: Type II
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Products

Affected productsLot or serial numberModel or catalog number
Single Use Guide Sheath KitAll lots.K-202
K-204
K-203
K-201

Issue

Olympus conducted an investigation into the Single Use Guide Sheath Kits after receiving complaints that the radiopaque tip of the guide sheath component fell off into the patient. Since July 2021, Olympus has received 32 complaints involving intraoperative disassociation of the guide sheath radiopaque tip in which the tip fell off into the patient. Of these 32 complaints, 26 were reported as serious injuries, and 6 were reported as malfunctions. The preliminary findings from Olympus' investigation have identified that the disassociation of the tip from the guide sheath is likely the result of excessive force applied when inserting instruments into the guide sheath, and/or damage to the distal end of the sheath. Olympus reminds users to closely follow the Instructions For Use (IFU) for the Single Use Guide Sheath Kits, especially the inspection directions detailed in sections 9 to 9.2 of the IFU, and the warnings and cautions listed in section 9.3 operation, which instruct users not to force instruments if resistance is encountered. Forcing instruments through the guide sheath can contribute to disassociation of the guide sheath radiopaque tip. Recall Start Date: January 15, 2025

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