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Glidesheath slender® introducer sheath
Official notice
2 Jul 2026
Last checked
2 Jul 2026
An official Health Canada notice concerns Glidesheath slender® introducer sheath. 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. Published 2026-07-02.
What to do now
Contact the manufacturer if you require additional information
Recall number
82268
Official notice
2026-07-02
The hazard
The hazard
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.
How to check if you're affected
How to check if you're affected
Compare the VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.
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The source does not list specific retailers. See the official notice for where affected vehicles were sold.
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Brand: Terumo Medical.
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Source & status
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Recall details
Recall details
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Documents, notices & source
See the official notice and source documents for full details.
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