Ferno-Washington Inc recalls Power F2 Powered Fastening System
- Recalling company
- Ferno-Washington Inc
- Product
- 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
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Apr 28, 2026
- Reported
- Oct 21, 2026
- Distribution
- 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.
- Status
- Ongoing
- Quantity
- 319
- Lot / codes
- 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 26C234
- Company location
- Wilmington, OH
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0145-2027
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0145-2027 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.