FERNO POWER X1 AMBULANCE COT
Medical device recall Z-0184-2023. Published in FDA’s Enforcement Report on Nov 16, 2022.
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 Nov 16, 2022. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 1,922 units 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?
Batteries could become unstable when not properly maintained and/or subjected to repeated drops, power washing directly into battery contacts or abuse, may result in a fire and/or injury
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V Li-Ion Batteries Model Number #0822484/0822483 Note: Transcend Stair Chair Powertraxx (Item #0731403/UDI-DI 00190790004064) not included in this action).
1,922 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
36V Li-Ion Battery: 00190790005474 (UDI N/A; GTIN ONLY) ALL SERIAL NUMBERS MANUFACTURED DURING AND PRIOR TO YEAR 2021, WEEK 15 (e.g. Serial # 20300102115M594). Ferno POWER X1 Ambulance Cot Serial Numbers (SN): 18F003862 18F003863 18F003864…
Every code shown here, 2,000 characters
36V Li-Ion Battery: 00190790005474 (UDI N/A; GTIN ONLY) ALL SERIAL NUMBERS MANUFACTURED DURING AND PRIOR TO YEAR 2021, WEEK 15 (e.g. Serial # 20300102115M594). Ferno POWER X1 Ambulance Cot Serial Numbers (SN): 18F003862 18F003863 18F003864 18F003865 18F003866 18F003867 18F003868 18F003869 18F003870 18F003871 18F003872 18F003873 18F003874 18F003875 18F003876 18F003877 18F003878 18F003879 18F003880 18F003881 18F003882 18F003883 18F003884 18F003893 18F003894 18F003895 18F003896 18F003897 18F003898 18F003899 18F003900 18F003921 18F003922 18F003923 18F003924 18F003925 18F003926 18F003927 18F003928 18F003930 18F003931 18F003932 18F003933 18F003934 18F003935 18F003936 18F003937 18F003940 18F003941 18F003942 18F003943 18F003944 18F003945 18F003946 18F003947 18F003950 18F003951 18F003952 18F003953 18F003954 18F003955 18F003956 18F003957 18F003958 18F003959 18F003960 18F003961 18F003962 18F003963 18F003964 18F003965 18F003966 18F003967 18F003968 18F003969 18F003970 18F003971 18F003972 18F003973 18F003974 18F003975 18F003976 18F003979 18F003980 18F003981 18F003982 18F003983 18F003984 18F003985 18F003986 18F003987 18F003988 18F003989 18F003990 18F003991 18F003992 18F003993 18F003994 18F003995 18F003996 18F003997 18F003998 18F003999 18F004000 18F004001 18F004002 18F004004 18F004005 18F004006 18F004007 18F004008 18F004009 18F004010 19F003932 19F004501 19F004502 19F004503 19F004504 19F004505 19F004506 19F004507 19F004508 19F004509 19F004512 19F004513 19F004514 19F004515 19F004516 19F004517 19F004518 19F004519 19F004520 19F004521 19F004522 19F004523 19F004524 19F004525 19F004526 19F004527 19F004528 19F004537 19F004538 19F004539 19F004540 19F004541 19F004542 19F004547 19F004548 19F004549 19F004550 19F004551 19F004552 19F004553 19F004554 19F004555 19F004556 19F004557 19F004558 19F004559 19F004560 19F004561 19F004562 19F004563 19F004564 19F004565 19F004566 19F004567 19F004568 19F004569 19F004570 19F004571 19F004572 19F004573 19F004574 19F004575 19F004576 19F004577 19F004578 19F004579…
FDA’s list runs to 19,429 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.
Nationwide Foreign: BRAZIL BRUNEI CHILE CHINA PERU POLAND PUERTO RICO TURKS&CACOS
These words name no state.
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 Oct 7, 2022.
- FDA classified it on Nov 4, 2022.
- FDA’s Enforcement Report published it on Nov 16, 2022.
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 19,429 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
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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.