Trevo XP Provue Retriever (2020-09-28)

Starting date:

September 28, 2020

Posting date:

October 6, 2020

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type I

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-74077

Last updated:
2020-10-06

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  Reason
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  Affected products

Affected Products

Trevo XP Provue Retriever

Reason

Stryker Neurovascular has observed an increase in complaints involving fractures of the core wires of the Trevo XP ProVue Retriever for certain lots manufactured between the time period of 22-Jul-2019 to 09-Sep-2019 resulting in stent retriever separation from the core wire during use.

Affected products