Recall archive / NHTSA
REV AMBULANCE TYPE I (2020) - Recall 24V281000 — NHTSA record 269997
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 Apr 19, 2024. 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 (2020) - Recall 24V281000
- Reason
- REV Ambulance Group Orlando, Inc. (REV) is recalling certain 2019-2024 Type I, Type III, and Type IX vehicles equipped with certain Weldon Vmux HC1.7 Input/Output multiplex nodes. In the event of a short circuit or wiring failure, the firmware in the node 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
- 76
- Agency-reported status
- Published safety recall
- Source record identifier
- 269997
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Product applicability: REV AMBULANCE TYPE I; model year 2020. 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
- Apr 19, 2024
- Owner notification
- May 17, 2024
- Record created
- Apr 19, 2024
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.