Public recall detail

Inzone® Detachment System

2026-09-24

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Health products Health product recall
Quick summary

Quick summary: Inzone® Detachment System. Reason: Health product recall. Category: Health products. Date: 2026-09-24.

Recommended action

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

Recall details

Quick summary: Inzone® Detachment System. Reason: Health product recall. Category: Health products. Date: 2026-09-24.

Official details

Affected product details

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

BrandStryker Neurovascular
ProductInzone® Detachment System
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82677

Affected products

ProductInzone® Detachment System
LotMore than 10 numbers, contact manufacturer.
ModelM00345100950
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionInzone® Detachment System

Issue

Stryker has observed that some devices may experience premature battery drain. When this occurs, the devices may: not power on; power on with faint audible and visual indicators; be unable to detach a coil as intended.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Neurology
CompaniesStryker Neurovascular 47900 Bayside Parkway, Fremont, California, United States, 94538
Recall date2026-09-11
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82677
Background{}
CompaniesStryker Neurovascular 47900 Bayside Parkway, Fremont, California, United States, 94538
AudiencesHealthcare
Source updated2026-09-24

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

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