FDA Recalls Power F2 Fastening Systems Over Rail Wear Risk
The FDA is recalling 278 Power F2 Powered Fastening Systems made by Ferno-Washington Inc due to potential roller wear and rail deformation that could prevent stretcher movement.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: This is an FDA Class II recall involving a medical device used in patient transport where mechanical failure could delay emergency care. Per the rubric, FDA Class II recalls with potential for serious health consequences are classified as Severe (Score 4).
Plain-English summary
The U.S. Food and Drug Administration (FDA) has issued a Class II recall of the Power F2 Powered Fastening System, Product No. 0567091, manufactured by Ferno-Washington Inc. A total of 278 units are affected by this recall.
The recalled device 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, preventing movement of the stretcher along the rail through either powered or manual operation. This may cause delays in transporting a patient to a healthcare facility.
The affected units were distributed nationwide in the United States and internationally in several countries including Poland, Netherlands, Canada, Germany, Norway, United Kingdom, Denmark, and New Zealand. The recall includes specific serial numbers listed under the UDI-DI 00190790006570.
Healthcare facilities and professional users who have the recalled Power F2 Powered Fastening Systems should immediately stop using the affected devices and contact Ferno-Washington Inc to arrange for inspection and repair or replacement. Users should follow any instructions provided by the manufacturer regarding alternative equipment during the remediation process.
The recalled product
- Product
- Power F2 Powered Fastening System, Product No. 0567091 Powered fastening system intended for professional use only. Designed to load, unload, and secure a compatible wheeled stretcher inside a ground-based ambulance. Item no. 0567091
- Manufacturer
- Ferno-Washington Inc
- Hazard
- mechanical-failure
- transport-delay
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- HighHalyard STANDARD LINE INSERTION PACK Recall for Silicone Seal Defect
FDA (Devices) · 2026-07-29
- SevereMEDLINE Medical Procedure Kits Containing Bupivacaine Recalled Due to Drug Ineffectiveness
FDA (Devices) · 2026-07-29
- HighFARADRIVE STEERABLE SHEATH CLEAR Medical Device Recall
FDA (Devices) · 2026-07-29
- HighBoston Scientific Recalls FARASTAR Ablation Generators Due to Catheter Incompatibility
FDA (Devices) · 2026-07-29
- HighPenumbra System RED 68 Reperfusion Catheter Recall Due to Fracture Risk
FDA (Devices) · 2026-07-29