Demers Ambulances FXP174 (2025) - Recall 26V098000 — NHTSA record 326187

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 Feb 20, 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
Demers Ambulances FXP174 (2025) - Recall 26V098000
Reason
Braun Industries, Inc. (Braun Ambulances) is recalling certain 2025-2026 Demers FXP174 ambulances. The floor may have insufficient strength to secure the seats in position during a crash. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard numbers 207, "Seating Systems" and 210, "Seat Belt Assembly Anchorages." Structural failure may prevent the seat from properly restraining an occupant during a crash, increasing the risk of injury.
Classification
Not supplied
Recalling firm
Braun Industries, Inc.
Quantity
7
Agency-reported status
Published safety recall
Source record identifier
326187

Open the official record

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityProduct applicability: Demers Ambulances FXP174; 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
Feb 20, 2026
Record created
Feb 20, 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.

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