Health product recall

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

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

Trevo XP Provue Retriever

Lot or serial number

30415
30416

Model or catalog number

90185

Companies
Manufacturer

Stryker Neurovascular

47900 Bayside Parkway

Fremont

94538

California

UNITED STATES