Ferno-Washington Inc recalls Power F2 Powered Fastening System
Reason for recall
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.
Affected product
Check your device
Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.
Affected products & lots
- 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.0567091UDI-DI 00190790006570277 affected lots25C22768725C22820426C23238226C23309125C22768825C22820526C23238326C233092
+269 more
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
What the firm is doing
On June 19. 2026, the firm began notifying customers via Urgent Medical Device Correction letters. Customers were instructed to contact Ferno for assistance if abnormal rail movement, increased resistance during rail extension or retraction, or other unusual rail operation is observed. Ferno will contact all affected customers directly and dispatch trained field service personnel to perform the correction onsite at customer locations. The correction does not require removal of the PF2 Fastening System from service prior to the scheduled repair. The field correction consists of replacement of the affected roller assembly with an updated assembly manufactured in accordance with revised assembly requirements intended to eliminate the potential for interference and subsequent roller deformation.
DistributionShow detailsHide
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.
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-2760-2026
- FDA device classification · FPOOfficial FDA classification for this device type
- CFR regulation · 21 CFR 880.6910The federal regulation governing this device
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find Ferno-Washington IncSearch for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.
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