Recall archive / NHTSA
REV AMBULANCE TYPE I (2023) - Recall 23V873000 — NHTSA record 249874
Published notice; closure not supplied
A campaign record does not say whether this individual vehicle has received the remedy. Check the VIN with NHTSA or the manufacturer.
Source date Dec 21, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- REV AMBULANCE TYPE I (2023) - Recall 23V873000
- Reason
- REV Ambulance Group Orlando, Inc. (REV) is recalling certain 2020-2024 Type I, III and IX vehicles. In the event of a short circuit or wiring failure, the firmware may fail to shut off the output pin, resulting in overloaded electrical circuits. Overloaded electrical circuits can overheat, increasing the risk of fire.
- Classification
- Not supplied
- Recalling firm
- REV Ambulance Group Orlando, Inc.
- Quantity
- 210
- Agency-reported status
- Published safety recall
- Source record identifier
- 249874
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Product applicability: REV AMBULANCE TYPE I; model year 2023. Check the model identifiers and, for a vehicle, the VIN on the official recall site. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Not supplied
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report received
- Dec 21, 2023
- Owner notification
- Jan 15, 2024
- Record created
- Dec 26, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.