REV AMBULANCE TYPE IX (2024) - Recall 24V281000 — NHTSA record 269992

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 IX (2024) - 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
269992

Open the official record

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityProduct applicability: REV AMBULANCE TYPE IX; model year 2024. 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.

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