The Recall Desk

Hazard

Failure To Detect recalls

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

What the numbers show

Total
3
Critical
0
Severe
1
Most recent
2025-09-08

Of the 3 failure to detect recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (33%) 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 failure to detect 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.

1–3 of 3

  • HighNHTSA·25V585000·2025-09-08

    2025 Rivian R1S and R1T Recalled Due to Software Defect

    Rivian is recalling certain 2025 R1S and R1T vehicles because the Hands-Free Highway Assist software may fail to detect lead vehicles, increasing crash risk. A free over-the-air software update is available.

    Product
    RIVIAN — RIVIAN R1S, R1T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2347-2012·2012-09-19

    Philips HeartStart MRx Monitor Defibrillators Recalled for Cable Wear

    Philips is recalling HeartStart MRx monitor/defibrillators because wear on the therapy cable connection may cause the device to fail to detect defibrillation pads or paddles.

    Product
    Philips HeartStart MRx monitor/defibrillators Models: M3535A and M3536A, M3536J, M3536M, M3536MC, M3536M1, M3536M2, M3536M3, M3536M4, M3536M5, M3536M6 The Heartstart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·04534·2004-02-12

    GE Security Recalls Carbon Monoxide Alarms Due to Software Error

    GE Security is recalling approximately 74,000 carbon monoxide alarms that fail to detect carbon monoxide after one year due to a software error.

    Product
    Carbon Monoxide (CO) Alarms
    Category
    Consumer Product
    Distribution
    Distributed nationwide