REV Ambulance Group Orlando, Inc.
Summary
NHTSA campaign 24V468: REV Ambulance Group Orlando, Inc. recalled for a safety defect. A detached module box or outrigger failure increases the risk of injury.
Details
Source
nhtsa
External ID
24V468
Action Date
2024-06-21
Status
Ongoing
Category
vehicle
Product Description
REV Ambulance Group Orlando, Inc. (REVO) is recalling certain 2019-2024 Type I and Type IX emergency vehicles equipped with outriggers. The outrigger bolts may not be properly tightened, which can cause the module box to detach, or cause failure of the outrigger.
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.
Want to know the moment something like this happens?
Get alerts for vehicle