REV Ambulance Group Orlando, Inc.
Summary
NHTSA campaign 21V289: REV Ambulance Group Orlando, Inc. recalled for a safety defect. A locked up or non-functional LCD display can delay emergency efforts, which can increase the risk of injury.
Details
Source
nhtsa
External ID
21V289
Action Date
2021-04-26
Status
Ongoing
Category
vehicle
Product Description
REV Ambulance Group Orlando, Inc. (REV) is recalling certain 2019-2021 Type I and IX vehicles equipped with Weldon V-Mux Vista IV LCD displays used for controlling emergency vehicle lighting and HVAC functions. These displays may experience low voltage spikes, causing the LCD display to lock up or become nonfunctional, due to varying electrical installations.
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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