6507 Power Pro 2
Brand(s)
Last updated
Summary
Product
6507 Power Pro 2
Issue
Medical devices - Performance
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
Get notified
Receive notifications for new and updated recalls and alerts by category.