Braun Ambulances
Summary
NHTSA campaign 23V331: Braun Ambulances recalled for a safety defect. The loss of rear brake function can increase the risk of a crash.
Details
Source
nhtsa
External ID
23V331
Action Date
2023-05-09
Status
Ongoing
Category
vehicle
Product Description
Braun Ambulances (Braun) is recalling certain 2019-2023 Chief XL Type I, Express Plus Type I, and Liberty Type I ambulances built on Chevrolet medium and heavy-duty chassis. The Liquid Spring suspension systems may come in direct contact with the right rear brake line, causing excessive wear and possibly resulting in the loss of the rear brakes.
Company
Context & Analysis
Braun Ambulances has 10 FDA actions in our database.
Frequently Asked Questions
How often does Braun Ambulances have FDA actions?
Braun Ambulances has 10 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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