Halcore Group, Inc.
Summary
NHTSA campaign 26V533: Halcore Group, Inc. recalled for a safety defect. A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash. Ino
Details
Source
nhtsa
External ID
26V533
Action Date
2026-08-17
Status
Ongoing
Category
vehicle
Product Description
Halcore Group, Inc. (Halcore) is recalling certain 2025-2026 Horton Type I, Type III, and Critical Care ambulances. The touchscreen display may stop responding to touch commands or fail to power on, preventing the activation of exterior emergency lights, as well as fire fighting and other emergency equipment.
Company
Context & Analysis
Halcore Group, Inc. has 2 FDA actions in our database.
Frequently Asked Questions
How often does Halcore Group, Inc. have FDA actions?
Halcore Group, Inc. has 2 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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