Health product recall

6507 Power Pro 2

Brand(s)
Last updated

Summary

Product
6507 Power Pro 2
Issue
Medical devices - Performance issue
What to do

Contact the manufacturer if you require additional information.

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalogue number
6507 Power Pro 2, High Config More than 10 numbers, contact manufacturer. 650705550001
6507 Power Pro 2, Mid Config 2211003786 2211003736 2211003737 2211003725 2211003726 2211003742 2211003768 2211003734 2211003752 2211003763 650705550002

Issue

Stryker has identified that the base leg assembly may bend. It was discovered that the variability in the manufacturing process at a tier 2 supplier may have results in low tensile strength of material. Bent base leg assembly may result in difficulty engaging/disengaging from fastener, difficulty loading/unloading from ambulance, difficulty raising or lowering the cot, cot tip, or erratic or unintended motion.

Recall start date: May 26, 2023

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies

Stryker Medical

3800 E Centre Avenue, Portage, Michigan, United States, 49002

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-73760

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