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The official notice did not include a photo. Check the product details and identifiers below.
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Glidesheath slender® introducer sheath
Official notice
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 product name and identifiers below with the item you own. Follow the official notice if they match.
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The source does not list specific retailers. See the official notice for where affected products were sold.
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Company & contacts
Brand: Terumo Medical.
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Source & status
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