Public recall detail

XCEL™ Bladeless Trocar

2026-10-01

medium
Gastroenterology and urology Type II
Quick summary

Quick summary: XCEL™ Bladeless Trocar . Reason: Type II. Category: Gastroenterology and urology. Date: 2026-10-01.

Recommended action

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

Recall details

Quick summary: XCEL™ Bladeless Trocar . Reason: Type II. Category: Gastroenterology and urology. Date: 2026-10-01.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandStryker Sustainability Solutions
ProductXCEL™ Bladeless Trocar
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82695

Affected products

ProductXCEL Bladeless Trocar W/Stability Sleeve
LotMore than 10 numbers, contact manufacturer.
ModelB11LT
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionXCEL Bladeless Trocar W/Stability Sleeve
ProductXCEL Bladeless Trocar W/Stability Sleeve
LotMore than 10 numbers, contact manufacturer.
ModelB12LT
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionXCEL Bladeless Trocar W/Stability Sleeve
ProductXCEL Bladeless Trocar W/Optiview Technology & Sleeve
LotMore than 10 numbers, contact manufacturer.
Model2B5LT
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionXCEL Bladeless Trocar W/Optiview Technology & Sleeve
ProductXCEL Bladeless Trocar W/Optiview Technology & Sleeve
LotMore than 10 numbers, contact manufacturer.
Model2B5ST
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionXCEL Bladeless Trocar W/Optiview Technology & Sleeve

Issue

Stryker has identified an increased number of complaints involving certain reprocessed Trocar devices, where the obturator assembly may crack or separate during use.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Gastroenterology and urology
CompaniesStryker Sustainability Solutions 1810 West Drake Dr., Tempe, Arizona, United States, 85283
Recall date2026-08-17
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82695
Background{}
CompaniesStryker Sustainability Solutions 1810 West Drake Dr., Tempe, Arizona, United States, 85283
AudiencesHealthcare
Source updated2026-10-01

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

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