Power F2 Powered Fastening System, Product No. 0567091 Powered fastening system intended for professional use…
Medical device recall Z-2760-2026. Published in FDA’s Enforcement Report on Jul 29, 2026.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Jul 29, 2026. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word, and 33 states named
- 278 how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“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.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
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.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
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
278, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
UDI-DI 00190790006570 Serial Numbers: 25C227687 25C228204 26C232382 26C233091 25C227688 25C228205 26C232383 26C233092 25C227689 26C231797 26C232384 26C233093 25C227690 26C231798 26C232709 26C233094 25C227691 26C231799 26C232710 26C233095…
Every code shown here, 1,998 characters
UDI-DI 00190790006570 Serial Numbers: 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 25C227702 26C232011 26C233035 26C233116 25C227703 26C232374 26C233036 26C233117 25C227704 26C232375 26C233037 26C233118 25C227707 26C232377 26C233038 26C233119 25C227708 26C232378 26C233039 26C233120 25C227709 26C232379 26C233040 26C233443 25C227710 26C232380 26C233041 26C233444 25C227711 26C232381 26C233090 26C233446 26C233448 26C234080 26C234360 26C234647 26C233449 26C234081 26C234361 26C234648 26C233450 26C234082 26C234362 26C234649 26C233451 26C234083 26C234363 26C234797 26C233452 26C234084 26C234364 26C234798 26C233692 26C234085 26C234566 26C234799 26C233693 26C234086 26C234567 26C234800 26C233694 26C234087 26C234630 26C234801 26C233695 26C234088 26C234631 26C234802 26C233696 26C234089 26C234632 26C234804 26C233697 26C234090 26C234633 26C234805 26C233698 26C234345 26C234634 26C234806 26C233699 26C234346 26C234635 26C234807 26C233700 26C234349 26C234636 26C234808 26C233701 26C234350 26C234637 26C234809 26C234071 26C234351 26C234638 26C234810 26C234072 26C234352 26C234639 26C234811 26C234073 26C234353 26C234640 26C234812 26C234074 26C234354 26C234641 26C234813 26C234075 26C234355 26C234642 26C234814 26C234076 26C234356 26C234643 26C234815 26C234077 26C234357 26C234644 26C234816 26C234078 26C234358 26C234645 26C235036 26C234079 26C234359 26C234646 26C235037 26C235038 26C235140 26C235437 26C235699 26C235039 26C235141 26C235438 26C235700…
FDA’s list runs to 2,807 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
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.
The states and territories these words name
33 states and territories.
Every one of them
- Alabama
- Arkansas
- Arizona
- California
- Georgia
- Iowa
- Idaho
- Illinois
- Indiana
- Kentucky
- Louisiana
- Maryland
- Maine
- Minnesota
- Missouri
- Montana
- North Carolina
- Nebraska
- New Jersey
- New Mexico
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- South Carolina
- Tennessee
- Texas
- Utah
- Virginia
- Washington
- Wisconsin
- West Virginia
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
The words say it went outside the United States too.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Jun 19, 2026.
- FDA classified it on Jul 17, 2026.
- FDA’s Enforcement Report published it on Jul 29, 2026.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Ferno-Washington Inc, of Wilmington, OH.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 2,807 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.