Power F2 Powered Fastening System, Power F2
Medical device recall Z-0145-2027. Published in FDA’s Enforcement Report on Oct 21, 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 Oct 21, 2026. Copied from openFDA on Oct 27, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word, and 30 states named
- 319 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?
Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to the system not operating in powered mode, or exhibiting reduced powered performance. Issue may result in interruption or delay in patient transport.
FDA, Device recall enforcement reports. Released Oct 27, 2026. Updated weekly.
Which ones are recalled?
Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X2, Item No. 0015816 and PowerX2 Premium, Item No. 0015821
319, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 27, 2026. Updated weekly.
Codes to check against yours
Power F2 UDI-DI 00190790006570 Firmware versions: PF2 Carriage V0.51/V1.42, PF2 Rail V0.41, PF2 Connect V108 Serial Numbers 25C227687 25C228205 25C228204 25C227690 25C227691 25C227692 25C227688 25C227689 25C227695 25C227700 25C227698…
Every code shown here, 1,994 characters
Power F2 UDI-DI 00190790006570 Firmware versions: PF2 Carriage V0.51/V1.42, PF2 Rail V0.41, PF2 Connect V108 Serial Numbers 25C227687 25C228205 25C228204 25C227690 25C227691 25C227692 25C227688 25C227689 25C227695 25C227700 25C227698 25C227699 25C227702 25C227703 25C227704 25C227696 25C227701 25C227710 25C227708 25C227711 26C231799 26C231800 26C231801 25C227709 25C227707 26C231797 26C232002 26C232004 26C232007 26C232005 26C232008 26C232009 26C231798 26C232010 26C232006 26C232011 26C232374 26C232377 26C232375 26C232379 26C232378 26C232382 26C232717 26C232715 26C232380 26C232384 26C232710 26C232713 26C233032 26C232381 26C232712 26C232718 26C232716 26C233035 26C232714 26C233033 26C233038 26C233041 26C233090 26C233040 26C233039 26C233037 26C233092 26C233036 26C233091 26C233094 26C233111 26C232711 26C233098 26C233097 26C233095 26C233096 26C233115 26C233114 26C233099 26C233113 26C233112 26C233117 26C233443 26C233119 26C233120 26C233118 26C233444 26C233451 26C233450 26C233449 26C233452 26C233692 26C233694 26C233693 26C233697 26C233699 26C233696 26C233701 26C233700 26C234074 26C234078 26C234072 26C234073 26C234076 26C233698 26C234077 26C234079 26C234080 26C234081 26C234082 26C234083 26C234071 26C234084 26C234085 26C234087 26C234086 26C234088 26C234356 26C234346 26C234353 26C234566 26C234352 26C234357 26C234361 26C234359 26C234355 26C234350 26C234362 26C234630 26C234363 26C234364 26C234649 26C234639 26C234632 26C234634 26C234631 26C234635 26C234648 26C234641 26C234640 26C234644 26C234646 26C234642 26C234647 26C234799 26C234797 26C234800 26C234805 26C234812 26C234567 26C234807 26C234801 26C234806 26C234810 26C234804 26C234808 26C234811 26C234814 26C234636 26C234809 26C235037 26C234813 26C234815 26C234816 26C235036 26C235045 26C235047 26C235048 26C235044 26C235046 26C235041 26C235049 26C235050 26C235052 26C235053 26C235054 26C235139 26C235135 26C235137 26C235055 26C235136 26C235138 26C235143 26C235134 26C235141 26C235142 26C235140 26C235144 26C235147 26C235151 26C235149…
FDA’s list runs to 6,821 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, CO, FL, ID, IL, KY, LA, ME, MN, MO, MT, NC, NE, NJ, NM, NY, OH, OK, PA, SC, TN, TX, UT, VA, WA, WI, WV and the countries of Netherlands and Poland.
The states and territories these words name
30 states and territories.
Every one of them
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Florida
- Idaho
- Illinois
- Kentucky
- Louisiana
- Maine
- Minnesota
- Missouri
- Montana
- North Carolina
- Nebraska
- New Jersey
- New Mexico
- New York
- Ohio
- Oklahoma
- 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 Apr 28, 2026.
- FDA classified it on Oct 9, 2026.
- FDA’s Enforcement Report published it on Oct 21, 2026.
FDA, Device recall enforcement reports. Released Oct 27, 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 27, 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 6,821 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 27, 2026 and checked Oct 27, 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 27, 2026.