Ferno-Washington Inc Power F2 Powered Fastening System, Power F2 recall: Firmware issue may result in intermittent loss or degradation of powered
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.
The hazard: Potency, impurity or stability failure
An out-of-specification result prompted this notice — potency, an impurity, or stability over the shelf life.
What the notice says: 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.
Why it matters: The product failed a specification test: it may contain more or less active ingredient than the label states, carry an impurity, or degrade before its expiry date. A sub-potent dose can leave a condition untreated; a super-potent one can cause an overdose.
Symptoms and when to call a doctor
The risk depends entirely on the drug. For a medicine where dose matters closely — a blood thinner, an anti-epileptic, a thyroid or heart medicine, insulin — talk to your prescriber before changing anything. Seek urgent care if you have symptoms that suggest too much drug, or if the condition the medicine controls starts breaking through.
This page is general information, not medical advice. If you feel unwell, a clinician who can see you is the only person able to judge your case.
Recall details
- Recall number
- Z-0145-2027
- Published
- October 21, 2026
- Risk level
- Class II
- Status
- Ongoing
- Issued by
- U.S. Food and Drug Administration
- Brand
- Ferno-Washington Inc
- Product type
- Medical devices
- Units affected
- 319
- Distribution
- Nationwide
- Made in
- United States
- Lot / code info
- 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 26C235150 26C235146 26C235148 26C235145 26C235152 26C235431 26C235429 26C235433 26C235432 26C235434 26C235438 26C235437 26C235436 26C235443 26C235446 26C235444 26C235445 26C235686 26C235447 26C235687 26C235700 26C235693 26C235696 26C235688 26C235692 26C235695 26C235697 26C235698 26C235699 26C235702 26C235694 26C235705 26C235701 26C236027 26C235703 26C236029 26C236030 26C236032 26C236035 26C235704 26C236028 26C236038 26C236039 26C236037 26C236042 26C236036 26C236034 26C236033 26C236040 26C236041 26C236026 26C236107 26C236109 26C236110 26C236043 26C236044 26C236045 26C236105 26C236108 26C236106 26C236116 26C236119 26C236113 26C236112 26C236244 26C236121 26C236245 26C236122 26C236123 26C236246 26C236250 26C236255 26C236118 26C236247 26C236729 26C236124 26C236254 26C236257 26C236258 26C236249 26C236260 26C236262 26C236734 26C236256 26C236728 26C236735 26C236731 26C236736 26C236732 26C236733 26C236737 26C236741 26C236746 Power X2 UDI-DI 00190790003210 (Power X2) and 00190790006600 (PowerX2 Premium) Firmware versions PX2 V1.11/V1.18 Serial Numbers 25G036128 25G036612 25G036614 25G036801 25G036802 25G036803 25G036804 25G036827 25G036830 25G036833 25G036834 25G036835 25G036837 25G036836 25G036953 25G036954 25G036958 25G036959 25G036960 25G036961 25G036962 25G036963 25G036964 25G037067 25G037068 25G037071 25G037094 25G037072 25G037095 25G037098 25G037100 25G037161 25G037163 25G037217 25G037225 25G037226 25G037227 25G037228 25G037229 25G037285 25G037289 25G037288 25G037298 25G037299 25G037305 25G037338 25G037342 25G037337 25G037466 25G037467 25G037468 25G037470 25G037471 25G037472 25G037473 25G037474 25G037526 25G037596 25G037595 25G037623 25G037665 25G037691 25G037692 25G037705 25G037707 25G037703 25G037704 25G037706 25G037713 25G037770 25G037772 25G037774 25G037780 25G037781 25G037782 25G038074 25G038075 25G038076 25G038080 25G038081 25G038082 25G038079 25G038083 25G038084 25G038536 25G038088 25G038539 25G038540 25G038615 25G038616 25G038617 25G038618 25G038625 25G038627 25G0385…
- UPC codes
- 00190790006570, 00190790003210, 00190790006600
Products covered by this recall
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
Check your product
The notice names 5 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.
UPC / barcode
Read the twelve digits under the barcode on the package.
- 00190790006570
- 00190790003210
- 00190790006600
Model or item number
On the rating label, the box or the instruction sheet.
- 0567093
- 0015821
Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.
What to do about Potency
Ferno-Washington Inc — An out-of-specification result prompted this notice — potency, an impurity, or stability over the shelf life.
- Check the lot number on your pack against the codes listed above before you do anything else.
- Keep the carton and the leaflet — the lot number is usually printed only on the outer pack.
- Report any change in how the medicine is working to FDA MedWatch, which is where most of these signals originate.
- Do not stop a prescription on your own. For most conditions an uncertain dose is safer than no dose while you get advice.
What the company owes you
A recalled medicine is the manufacturer’s cost to carry, not yours or your pharmacist’s.
- The purchase price or co-pay is refundable, and so is the cost of returning the product if they ask you to ship it.
- Ask the pharmacy to handle the claim where they can — they process recall returns in bulk and it saves you the correspondence.
- Keep the carton, the leaflet and the pharmacy label together until the claim is closed.
- Costs beyond the price of the medicine need to go to the company directly, in writing, with the recall number quoted.
Company contact: Ferno-Washington Inc — 70 Weil Way, Wilmington, OH, 45177-9371
The official notice
This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.
Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls
Questions people ask about this recall
Why was Ferno-Washington Inc medical devices recalled?
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. 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.
How do I know if I have the recalled product?
Match the codes printed on your package against the notice: UPC 00190790006570, 00190790003210, 00190790006600; model number 0567093, 0015821. If the code on your package is not on that list, your unit is outside the recall.
What should I do with it right now?
Check the lot number on your pack against the codes listed above before you do anything else.
Can I get my money back?
The purchase price or co-pay is refundable, and so is the cost of returning the product if they ask you to ship it.
Where was the recalled product sold?
It was distributed nationwide.
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