Recall archive / NHTSA
HORTON TYPE I (2025) - Recall 26V533000 — NHTSA record 321410
Published notice; closure not supplied
A campaign record does not say whether this individual vehicle has received the remedy. Check the VIN with NHTSA or the manufacturer.
Source date Aug 14, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- HORTON TYPE I (2025) - Recall 26V533000
- Reason
- 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. A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash. Inoperative equipment can delay emergency response, increasing the risk of injury.
- Classification
- Not supplied
- Recalling firm
- Halcore Group, Inc.
- Quantity
- 545
- Agency-reported status
- Published safety recall
- Source record identifier
- 321410
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Product applicability: HORTON TYPE I; model year 2025. Check the model identifiers and, for a vehicle, the VIN on the official recall site. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Not supplied
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report received
- Aug 14, 2026
- Record created
- Aug 17, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.