FDA Device recall Z-0184-2023
FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V Li-Ion Batteries Model Number #0822484/0822483 Note: Transcend S…
- FDA Device
- Class II
- ongoing
- Published 2022-11-16
On 2022-11-16 the FDA classified a Class II recall of FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V Li-Ion Batteries Model Number #0822484/0822483 Note: Transcend S… by Ferno Washington, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0184-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-10-07 |
| Published | 2022-11-16 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Ferno Washington |
| Distribution | US |
Product
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).
Reason
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
Identifiers
| code_info | 36V Li-Ion Battery: 00190790005474 (UDI N/A; GTIN ONLY) ALL SERIAL NUMBERS MANUFACTURED DURING AND PRIOR TO YEAR 2021,…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 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0184-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.