Manufacturer
29 recalls in our database name Halcore Group, Inc. as the manufacturing or recalling firm.
Of the 29 recalls from Halcore Group, Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 11 (38%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Halcore Group is recalling 2025-2026 Horton ambulances because touchscreen failures may prevent emergency lights from activating, increasing crash risk.
Halcore Group, Inc. is recalling certain 2023–2024 Horton emergency vehicles built on Ford F-450, F-550, and F-600 chassis because the left rear brake line can contact and be damaged by the strut mount when the rear suspension is lowered, risking brake fluid leakage and loss of brakes.
Halcore is recalling specific 2020-2021 AEV ambulances because electrical spikes may cause the emergency lighting and HVAC control display to lock up or fail.
Halcore is recalling 2020 Horton Type I and III emergency vehicles because a display processor may stop working, potentially delaying emergency services.
Halcore Group is recalling 2019-2020 AEV TraumaHawk ambulances because rear brake lines may wear from contact with suspension parts, risking brake loss.
Halcore is recalling 2018-2020 Horton ambulances because a rear brake line may wear from contact with suspension parts, risking brake loss.
Halcore Group is recalling 2018 AEV Traumahawk ambulances because an undersized power cord may cause an electrical short circuit, increasing the risk of fire or shock.
Halcore Group is recalling 2016-2019 Horton Type I and III ambulances because an undersized A/C power cord may cause an electrical short circuit, increasing the risk of fire or shock.
Halcore is recalling 2018-2019 Horton Type I and Type III ambulances because the oxygen tank bracket may loosen, allowing the tank to become airborne in a crash.
Halcore Group is recalling 2018-2020 Horton Type I and III emergency vehicles because air bag cushions may detach and fail to inflate during a crash.
Halcore Group is recalling 2016-2019 AEV TraumaHawk ambulances because backup camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.
Halcore Group is recalling 2016-2019 Horton ambulances because backup camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.
Halcore is recalling 2017-2018 Horton Type I and Type III ambulances because Whelen accessory brake lights may illuminate without the brake pedal being pressed.
Halcore Group is recalling 2017-2018 AEV Traumahawk ambulances because Whelen accessory brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.
Halcore Group is recalling 2017 AEV Traumahawk ambulances because a battery isolator module may overheat, posing a fire and injury risk.
Halcore Group is recalling 2016-2017 AEV Traumahawk ambulances because door striker bolts may fail under load, potentially allowing doors to open in a crash.
Halcore Group is recalling 2017 Horton ambulances because overtightened rear brake bolts may cause loss of braking power, increasing crash risk.
Halcore Group is recalling 2017 AEV Traumahawk ambulances because overtightened rear brake bolts may cause loss of braking power, increasing crash risk.
Halcore Group is recalling 2016 AEV Traumahawk ambulances because Stryker Medical Performance cot mounts may not securely attach the cot, posing a risk of serious injury.
Halcore Group is recalling 2016-2017 AEV Traumahawk ambulances because defective seat tracks may cause the attendant seat to move rapidly during a crash, increasing injury risk.
Halcore Group is recalling 2013-2016 Horton ambulances because a poorly sealed air conditioner wire harness allows water entry, creating a risk of electrical fire.
Halcore is recalling 2006-2013 AEV Ambulance Wheelchair Vans because wheelchair lift bearings may move, causing the platform to fall and injure operators.
Halcore Group is recalling 18 model year 2015 Horton ambulances because an incorrectly installed circuit board component may cause electrical system failure, potentially disabling life-saving equipment.
Halcore is recalling 2008-2014 AEV Type II ambulances because the rearward-facing attendant seat belt cable may break, increasing injury risk in a crash.
Halcore Group is recalling 2014-2015 AEV Trauma Hawk emergency vehicles because the backup camera may display reversed images, increasing crash risk.