FDA recall record

Ferno-Washington Power F2 Powered Fastening System, Product No. 0567091 Powered fastening recall — FDA Z-2760-2026

Product may experience accelerated roller wear and potential deformation due to interference between the roller assembly and rail. In the worst-case…

Class IIclassification
Z-2760-2026official record ID
Jul 29, 2026report date

Recall record at a glance

Official recordZ-2760-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmFerno-Washington Inc
Report dateJul 29, 2026
Recall initiation dateJun 19, 2026
Quantity278
LocationWilmington, OH, United States

Official product description

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

Why the product 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.

Distribution information

Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, GA, IA, ID, IL, IN, KY, LA, MD, ME, MN, MO, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV and the countries of Poland, Netherlands, Canada, Germany, Norway, United Kingdom, Denmark and New Zealand.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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