The Recall Desk

Hazard

Evacuation Delay recalls

9 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9
Critical
0
Severe
0
Most recent
2026-02-04

Of the 9 evacuation delay recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all evacuation delay recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–9 of 9

  • HighNHTSA·26V063000·2026-02-04

    Mercedes-Benz Tourrider Buses Recalled for Door Control Valve Defect

    Daimler Coaches is recalling 2026 Mercedes-Benz Tourrider buses because a faulty door valve may prevent doors from opening, delaying emergency evacuation.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ TOURRIDER BUSINESS, TOURRIDER PREMIUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V441000·2024-06-14

    Thor Motor Coach Motorcoaches: Emergency Exit Window Obstruction Recall

    Thor Motor Coach is recalling 2023-2024 Magnitude and Omni motorcoaches because the emergency exit window can become blocked when the outside griddle is in use, potentially delaying evacuation during an emergency.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH OMNI, MAGNITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2422-2021·2021-09-15

    Philips Ingenia Ambition X MRI System Tabletop May Fail to Retract

    Philips Ingenia Ambition X MRI systems may have tabletops that fail to move completely in manual mode, potentially delaying patient evacuation from the scanner and treatment. The issue affects 147 units distributed worldwide.

    Product
    Ingenia Ambition X- Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Models:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2418-2021·2021-09-15

    MRI Magnetic Resonance System Tabletop May Fail to Move in Manual Mode

    Philips Ingenia Elition S-a MRI systems may have tabletop movement failure in manual mode, potentially delaying patient evacuation from the scanner bore and treatment. This affects 64 units distributed worldwide.

    Product
    Ingenia Elition S-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Models:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2414-2021·2021-09-15

    MRI Tabletop Movement Malfunction in Manual Mode Affects Philips Ingenia Systems

    Philips Ingenia 1.5T CX-a MRI systems may have a tabletop that fails to fully move in or out during manual operation, potentially delaying patient evacuation and treatment.

    Product
    Ingenia 1.5T CX-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Models:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2411-2021·2021-09-15

    MRI diagnostic device tabletop may not move completely in manual mode

    Philips Ingenia 1.5T MRI systems may have a mechanical defect where the tabletop fails to move fully in and out during manual operation, potentially delaying patient evacuation and treatment.

    Product
    Ingenia 1.5T- a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Models: 781
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2413-2021·2021-09-15

    MRI device tabletop may fail to move completely in manual mode

    Philips Ingenia MRI tabletops may fail to move completely in manual mode, potentially delaying patient evacuation. The recall affects 144 units worldwide.

    Product
    Ingenia 1.5T S-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Model: 7813
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2421-2021·2021-09-15

    MRI Tabletop Movement Failure May Delay Patient Evacuation and Treatment

    Philips MRI systems may fail to move the examination tabletop in manual mode, potentially delaying patient evacuation and medical treatment.

    Product
    SmartPath to dStream for XR and 3.0T-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or ext
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V425000·2015-07-06

    Thomas Built Buses Recall Emergency Door Handle Corrosion Defect

    Daimler Trucks North America is recalling certain Thomas Built Buses because corrosion on the emergency door handle stem may delay evacuation during an emergency.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES, THOMAS SAF-T-LINER C2, SAF-T-LINER MVP-ER, SAF-T-LINER ER, SAF-T-LINER MVP-EF
    Category
    Vehicle
    Distribution
    Distributed nationwide