FDA recall, , Moderate risk
Ferno Power F2 Powered Fastening System
The Power F2 Powered Fastening System may experience accelerated roller wear and deformation, causing the rail to lodge and delaying patient transport.
Summary by Recall Canary from the FDA notice
What happened
Ferno-Washington Inc, of Wilmington, Ohio, began a recall of the Power F2 Powered Fastening System, Product No. 0567091, on June 19, 2026. The FDA added the recall to its Enforcement Report on July 17, 2026. The powered fastening system, intended for professional use, may experience accelerated roller wear and potential deformation due to interference between the roller assembly and rail.
In the worst-case condition, the rail mechanism may become lodged during operation and movement of the stretcher along the rail may no longer be possible through either powered or manual operation. The product was distributed nationwide in the United States and internationally, including in Poland, Netherlands, Canada, Germany, Norway, United Kingdom, Denmark and New Zealand.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the item number and UDI-DI listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
Power F2 Powered Fastening System
- Item number
- 0567091
- UDI-DI
- 00190790006570
Recall details
- Company began the recall
- Sold in
Worldwide - US Nationwide distribution in the states of Alabama, Arkansas, Arizona, California, Georgia, Iowa, Idaho, Illinois, Indiana, Kentucky, Louisiana, Maryland, Maine, Minnesota, Missouri, Montana, North Carolina, Nebraska, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and the countries of Poland, Netherlands, Canada, Germany, Norway, United Kingdom, Denmark and New Zealand.
- Company
- Ferno-Washington IncWilmington, Ohio
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99291
- Recall number
- Z-2760-2026
All recalls from Ferno-Washington Inc
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
