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Class IIOngoing

Ferno-Washington Inc recalls Power F2 Powered Fastening System

Recall date · record updated Oct 21, 2026 · Source: U.S. Food and Drug Administration (openFDA device enforcement)

What to do

Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.

Company
Ferno-Washington Inc
Reason
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.
Hazard
FDA Class II: may cause temporary or medically reversible adverse health consequences (FDA definition).
Who’s affected
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.
Where
Nationwide
Official notice
www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99861…

Products

  1. 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

    Codes/lots: 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 26C232Quantity: 319Recall no. Z-0145-2027Class II

Update history

  1. First listed on OVERLOOKED from the official record.

When the agency expands or changes this recall, we update this page and log the change here.

Proof: raw official record (JSON) · fetched from FDA API

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