REV Ambulance Group Orlando, Inc.
Summary
NHTSA campaign 24V281: REV Ambulance Group Orlando, Inc. recalled for a safety defect. Overloaded electrical circuits can overheat, increasing the risk of fire.
Details
Source
nhtsa
External ID
24V281
Action Date
2024-04-19
Status
Ongoing
Category
vehicle
Product Description
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.
Context & Analysis
REV Ambulance Group Orlando, Inc. has 4 FDA actions in our database.
Frequently Asked Questions
How often does REV Ambulance Group Orlando, Inc. have FDA actions?
REV Ambulance Group Orlando, Inc. has 4 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.
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