Reported Jul 29, 2026 · Ongoing · Updated Sep 16, 2026

Power F2 Powered Fastening System, Product No. 0567091 Powered fastening system intended for professional use only.…

Ferno-Washington Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Ferno-Washington Inc · 70 Weil Way · Wilmington, OH · 45177-9371

Is this the product you have?

  • 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
Lot codes and dates
  • UDI-DI 00190790006570 Serial Numbers

    277 of 277 codes

    • 25C227687
    • 25C228204
    • 26C232382
    • 26C233091
    • 25C227688
    • 25C228205
    • 26C232383
    • 26C233092
    • 25C227689
    • 26C231797
    • 26C232384
    • 26C233093
    • 25C227690
    • 26C231798
    • 26C232709
    • 26C233094
    • 25C227691
    • 26C231799
    • 26C232710
    • 26C233095
    • 25C227692
    • 26C231800
    • 26C232711
    • 26C233096
    • 25C227693
    • 26C231801
    • 26C232712
    • 26C233097
    • 25C227694
    • 26C232002
    • 26C232713
    • 26C233098
    • 25C227695
    • 26C232004
    • 26C232714
    • 26C233099
    • 25C227696
    • 26C232005
    • 26C232715
    • 26C233100
    • 25C227697
    • 26C232006
    • 26C232716
    • 26C233111
    • 25C227698
    • 26C232007
    • 26C232717
    • 26C233112
    • 25C227699
    • 26C232008
    • 26C232718
    • 26C233113
    • 25C227700
    • 26C232009
    • 26C233032
    • 26C233114
    • 25C227701
    • 26C232010
    • 26C233033
    • 26C233115
Amount recalled
278

Where it was sold

Why it was recalled

Product may experience accelerated roller wear and potential deformation due to interference between the roller assembly and rail. In the worst-case condition, 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. May cause delays in transport of patient to healthcare facility.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (Enforcement Report)

Read the FDA (weekly enforcement report) notice

Data as of Sep 19, 5:01 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.