The Recall Desk

Hazard

Cybersecurity recalls

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

What the numbers show

Total
30
Critical
1
Severe
1
Most recent
2026-01-28

Of the 30 cybersecurity recalls we have scored against our rubric, 1 (3%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (3%) 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 cybersecurity 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.

26–30 of 30

  • HighFDA (Devices)·Z-0035-2018·2017-10-25

    St Jude Medical Recalls 101 Implantable Pacemakers for Firmware Update

    St Jude Medical is recalling 101 implantable pacemaker pulse generators to install new firmware that mitigates the risk of unauthorized access via radio frequency communications.

    Product
    PM1226 ACCENT ST MRI SR RF and PM2222 ACCENT ST These low voltage (LV) devices are implantable pacemaker pulse generators, intended to be permanently implanted in the body, that have a power supply and electronic circuits that produce a periodic electrical pulse to stimulate the
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0038-2018·2017-10-25

    St Jude Medical Recalls Pacemakers for Firmware Security Update

    St Jude Medical is recalling 2,726 implantable pacemakers to install new firmware that mitigates the risk of unauthorized access via radio frequency communications.

    Product
    PM3544 QUADRA RELIEVE and PM3562 QUADRA ALLURE MP These low voltage (LV) devices are implantable pacemaker pulse generators, intended to be permanently implanted in the body, that have a power supply and electronic circuits that produce a periodic electrical pulse to stimulate t
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0036-2018·2017-10-25

    St Jude Medical Recalls ZENEX Pacemakers for Firmware Update

    St Jude Medical is recalling 4,828 ZENEX pacemakers to install new firmware that mitigates the risk of unauthorized access via radio frequency communications.

    Product
    PM 1250 and PM 2250 ZENEX; PM1282 and PM2282 ZENEX MRI These low voltage (LV) devices are implantable pacemaker pulse generators, intended to be permanently implanted in the body, that have a power supply and electronic circuits that produce a periodic electrical pulse to stimu
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·15V508000·2015-08-12

    Jeep Renegade Recall for Radio Software Vulnerability

    Chrysler is recalling 2015 Jeep Renegade vehicles to fix a radio software vulnerability that could allow unauthorized remote control of vehicle systems.

    Product
    JEEP — JEEP RENEGADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V461000·2015-07-23

    Chrysler Recalls 2013-2015 Vehicles for Radio Software Vulnerability

    Chrysler is recalling specific 2013-2015 Ram, Jeep, Dodge, and Chrysler vehicles because radio software vulnerabilities allow unauthorized remote access to vehicle control systems, increasing crash risk.

    Product
    RAM — RAM, JEEP, DODGE 5500, 1500, CHEROKEE, VIPER
    Category
    Vehicle
    Distribution
    Distributed nationwide