The Recall Desk

Hazard

Interlock Failure recalls

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

What the numbers show

Total
8
Critical
0
Severe
0
Most recent
2026-04-30

Of the 8 interlock failure 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 interlock failure 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.

1–8 of 8

  • HighCPSC·26450·2026-04-30

    Residential elevator StrikeLock devices may let the cab move with doors open

    StrikeLock hoistway door locking devices for residential elevators are recalled because they can allow the elevator cab to move with a landing door open, posing a fall hazard.

    Product
    Residential Elevators StrikeLock Hoistway Door Locking Device
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2105-2019·2019-08-14

    Comet Technologies Recalls YXLON Cheetah Cabinet X-Ray Systems

    Comet Technologies is recalling 77 YXLON Cheetah cabinet X-Ray systems because the door interlock fails to meet federal performance standards for power disconnection.

    Product
    YXLON Cheetah cabinet X-Ray System Product Usage: The products are generally used for non-destructive testing and quality control
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0705-2019·2019-01-16

    Mevion Medical Systems Recalls MEVION S250i Medical Device

    Mevion Medical Systems is recalling one MEVION S250i unit due to a dDose1 interlock trip. Treatment may continue via partials.

    Product
    MEVION S250i
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1480-2017·2017-03-22

    Philips BrightView Nuclear Imaging Systems Recalled for Motion and Software Issues

    Philips Medical Systems is recalling 1,218 BrightView nuclear imaging systems worldwide due to four issues, including motion controller failures and software freezes.

    Product
    882480: BrightView designed for single or dual detector nuclear imaging accommodating a range of ECT studies. In addition it can be used to perform planar static, dynamic, gated, total body, circular-orbit and noncircular orbit SPECT, gated SPECT (circular and noncircular)studies
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1197-2017·2017-02-22

    Advanced Sterilization Products Recalls STERRAD NX Sterilization Systems

    Advanced Sterilization Products is recalling STERRAD NX Sterilization Systems because the door interlock may disengage for 20 seconds after a power outage.

    Product
    STERRAD NX Sterilization System, Product Code: 10033, 10033-002
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0580-2015·2014-12-17

    Boston Scientific Recalls IntellaMap Orion Mapping Catheters Due to Glue Failure

    Boston Scientific is recalling 184 IntellaMap Orion High Resolution Mapping Catheters because a glue bond on the Deployment Interlock Button may fail.

    Product
    IntellaMap Orion High Resolution Mapping Catheter; Material number: M004RC64S0; Catalog number RC64S; Is indicated for electrophysiological mapping (recording or stimulating only) of the cardiac structures of the heart.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0464-2015·2014-12-03

    Vision RT AlignRT System Recalled for Potential Interlock Failure

    Vision RT is recalling AlignRT systems due to a potential failure to assert interlock, which could affect radiation safety during treatment.

    Product
    AlignRT- Intended for prescription use. The system is indicated for use during simulation, setup and stereotactic radiosurgery and precision radiotherapy for lesions, tumors and conditions anywhere in the body where radiation is indicated.
    Category
    Medical Device
    Distribution
    4 states
  • HighCPSC·06577·2006-08-29

    John Deere Recalls X300 Select Series Lawn Tractors Due to Blade Safety Issue

    Deere & Company is recalling about 16,000 John Deere X300 Select Series lawn tractors because a manufacturing defect could allow the blades to operate while the mower is unattended.

    Product
    John Deere X300 Select Series Lawn Tractors
    Category
    Consumer Product
    Distribution
    Distributed nationwide