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Use caution Medical device recall · FDA · Published June 19, 2026

Ferno-Washington Power F2 Powered Fastening System Recall: Roller Wear Risk

Ferno-Washington recalls Power F2 Powered Fastening System (Product No. 0567091) due to potential roller wear and rail deformation that may cause transport delays for patients.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2760-2026Medical deviceFerno-Washington ›
✎ GovInfoNow plain-language explainer

Ferno-Washington is recalling its Power F2 Powered Fastening System (Product No. 0567091) because it may experience accelerated roller wear and deformation, which could prevent proper movement of the stretcher during patient transport. This risk could delay critical healthcare delivery. Read more at govinfonow.com/recall/127766-ferno-washington-power-f2-powered-fastening-system-recall-roller-wear.

Source Summary by GovInfoNow · govinfonow.com/recall/127766-ferno-washington-power-f2-powered-fastening-system-recall-roller-wear · Updated August 10, 2026 · FDA enforcement record: FDA #Z-2760-2026

Cite this page

“Ferno-Washington Power F2 Powered Fastening System Recall: Roller Wear Risk.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/127766-ferno-washington-power-f2-powered-fastening-system-recall-roller-wear. Based on FDA recall #Z-2760-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2760-2026%22&limit=1).

The FDA announced on June 19, 2026, that Ferno-Washington Inc is recalling the Power F2 Powered Fastening System due to potential roller wear and deformation. The agency said the hazard may cause delays in patient transport if the rail mechanism becomes lodged.

How to tell if you have it

  • Brand: Ferno-Washington
  • Product: Power F2 Powered Fastening System, Product No. 0567091
  • Serial Numbers: 25C227687 through 26C235698 (as listed in record)
  • Distribution: US Nationwide and Poland, Netherlands, Canada, Germany, Norway, United Kingdom, Denmark, New Zealand

The hazard

The product 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, making movement of the stretcher along the rail impossible through either powered or manual operation. This may cause delays in transport of patient to healthcare facility.

Context

GovInfoNow's records show Ferno-Washington Inc has two other recalls on record since October 7, 2022. On September 11, 2025, the company recalled the Power X2 Ambulance Cot because the fastening post may detach. On October 7, 2022, Ferno-Washington recalled the Power X1 Ambulance Cot due to a fire risk if batteries were not properly maintained. Other recent recalls of similar products include the Reign Medical Clench Staple System (July 15, 2026), the Merit Medical Allwell Angioplasty Pack (December 4, 2025), and the Olympus HX-400U-30 Ligating Device (October 30, 2025).

How to tell if you have this one

Check for serial numbers listed in the recall notice: 25C227687 through 26C236253. The product is a powered fastening system for professional ambulance use only.

  • Brand
    Ferno-Washington
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Product Serial Numbers

    Verify if your unit has a serial number listed in the recall notice (25C227687 to 26C236253).

Where it went and when

Where it was distributed

Distributed nationwide and abroad; the notice names 33 states.

Alaska: nationwideAKMaine: named in the noticeMEVermont: nationwideVTNew Hampshire: nationwideNHWashington: named in the noticeWAIdaho: named in the noticeIDMontana: named in the noticeMTNorth Dakota: nationwideNDMinnesota: named in the noticeMNIllinois: named in the noticeILWisconsin: named in the noticeWIMichigan: nationwideMINew York: named in the noticeNYRhode Island: nationwideRIMassachusetts: nationwideMAOregon: named in the noticeORNevada: nationwideNVWyoming: nationwideWYSouth Dakota: nationwideSDIowa: named in the noticeIAIndiana: named in the noticeINOhio: named in the noticeOHPennsylvania: named in the noticePANew Jersey: named in the noticeNJConnecticut: nationwideCTCalifornia: named in the noticeCAUtah: named in the noticeUTColorado: nationwideCONebraska: named in the noticeNEMissouri: named in the noticeMOKentucky: named in the noticeKYWest Virginia: named in the noticeWVVirginia: named in the noticeVAMaryland: named in the noticeMDDelaware: nationwideDEArizona: named in the noticeAZNew Mexico: named in the noticeNMKansas: nationwideKSArkansas: named in the noticeARTennessee: named in the noticeTNNorth Carolina: named in the noticeNCSouth Carolina: named in the noticeSCDistrict of Columbia: nationwideDCOklahoma: named in the noticeOKLouisiana: named in the noticeLAMississippi: nationwideMSAlabama: named in the noticeALGeorgia: named in the noticeGAHawaii: nationwideHITexas: named in the noticeTXFlorida: nationwideFL

FDA distribution: “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,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Alabama, Arizona, Arkansas, California, Georgia, Idaho, Illinois, Indiana, Iowa, Kentucky, Louisiana, Maine, Maryland, Minnesota, Missouri, Montana, Nebraska, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin.

Recall timeline

FDA published this recall 40 days after the firm started it.

1. Firm started the recall: Jun 19, 202612. FDA classified it Class II: Jul 17, 202623. Published in FDA’s Enforcement Report: Jul 29, 202632026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-2760-2026 (June 19, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2760-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA