Quick summary: Glidesheath Slender® Introducer Sheath. Reason: Health product recall. Category: Health products. Date: 2026-07-02.
Glidesheath Slender® Introducer Sheath
2026-07-02
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: Glidesheath Slender® Introducer Sheath. Reason: Health product recall. Category: Health products. Date: 2026-07-02.
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
Affected products
Issue
Through post-market surveillance, we have received complaints for the guidewire not being able to pass through the needle. Through our investigation it was determined that a portion of the lot had the incorrect guidewire size. Terumo has received 84 complaints for this issue and no serious injuries. The probability of medically reversible or transient adverse health consequences is not likely. The situation is detectable at the time of use. There is no risk to patients who have used this lot. 1. Review your Glidesheath Slender inventory and immediately isolate lot number 0001441871.
What you should do
- Contact the manufacturer if you require additional information
Additional official information
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
Frequently asked questions
Answers based on the official recall notice.
Product images
Official product images from Health Canada.
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