Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X
Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to the system not operating in powered mode, or exhibiting reduced powered performance.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
Severity not yet assessed
We have not scored this recall against our rubric yet, so we are not showing a severity rating or our usual guidance. The agency’s own notice below is the authoritative source — read it first.
Plain-English summary
Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to the system not operating in powered mode, or exhibiting reduced powered performance. Issue may result in interruption or delay in patient transport.
The recalled product
- Product
- Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X2, Item No. 0015816 and PowerX2 Premium, Item No. 0015821
- Manufacturer
- Ferno-Washington Inc
- Category
- Medical Device — Devices
- Affected units
- 319
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Power F2 UDI-DI 00190790006570 Firmware versions: PF2 Carriage V0.51/V1.42
- PF2 Rail V0.41
Distribution
Related recalls
Same manufacturer · Ferno-Washington Inc
See all →- SevereFDA Recalls Power F2 Fastening Systems Over Rail Wear Risk
FDA (Devices) · 2026-07-29
- HighPowered ambulance cots recalled because fastening post hardware could loosen
FDA (Devices) · 2025-10-22
- HighFERNO POWER X1 ambulance cot batteries pose fire and burn risk
FDA (Devices) · 2022-11-16
- ModerateFerno Chair Cot Recalled Due to Incorrect Manufacturing Nut
FDA (Devices) · 2017-04-26
- ModerateFerno-Washington Recalls Traction Splint Straps Due to Incorrect Packaging Labels
FDA (Devices) · 2016-05-11