The Recall Desk

Hazard

Failure To Alert recalls

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

What the numbers show

Total
14
Critical
0
Severe
1
Most recent
2025-06-05

Of the 14 failure to alert 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 (7%) 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 alert 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.

1–14 of 14

  • SevereCPSC·25322·2025-06-05

    Apollo America Combination Smoke and Carbon Monoxide Detectors Recalled

    Apollo America 51000-600 combination smoke and carbon monoxide detectors can malfunction and fail to alert users to fire or CO leaks, risking smoke inhalation, CO poisoning, or death. Vivint is sending free replacement detectors to all known purchasers.

    Product
    Apollo America 51000-600 Combination Smoke and Carbon Monoxide Detectors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1656-2025·2025-04-30

    CELL-DYN Ruby hematology analyzer medical device recall

    Abbott Laboratories is recalling CELL-DYN Ruby hematology analyzers because expired reagents may be used without user notification when scanned or manually entered into the system, contrary to manufacturer guidelines.

    Product
    Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 04U42-84 Software Version: All software versions Product Description: CELL-DYN Ruby
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2417-2024·2024-07-31

    Call station devices may fail to transmit emergency alarms to staff

    Securitas Healthcare's Arial Call Station (models CSK200 and CSK200MR) may fail to transmit alarms and experience premature battery depletion. The FDA recall affects 1,268 units distributed in the U.S. and Canada.

    Product
    Arial Call Station, Model Numbers CSK200 and CSK200MR, is a wireless, battery-operated call device installed inside resident living areas to allow immediate staff response.
    Category
    Medical Device
    Distribution
    9 states
  • HighCPSC·20140·2020-06-17

    Edwards Recalls Mechanical Heat Detectors Due to Fire Alert Failure

    Edwards Fire Safety is recalling about 85,000 mechanical heat detectors that may fail to activate during a fire, posing a risk of failure to alert consumers.

    Product
    Edwards Mechanical Heat Detectors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20114·2020-04-30

    Bellman & Symfon Recalls Flash Receivers for Hearing-Impaired Users

    Bellman & Symfon is recalling Flash Receivers because the backup battery may fail to charge, preventing the unit from alerting hearing-impaired users to emergencies.

    Product
    Flash Receivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18128·2018-03-21

    Kidde Recalls Dual-Sensor Smoke Alarms Due to Manufacturing Defect

    Kidde is recalling about 452,000 dual-sensor smoke alarms in the U.S. because a manufacturing defect may prevent them from detecting smoke.

    Product
    Kidde dual-sensor (photoelectric and ionization) smoke alarms - models PI2010 and PI9010
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1499-2017·2017-03-29

    Stanley Security Recalls 500 Arial Wireless Call Pendants

    Stanley Security Solutions is recalling 500 Arial Wireless Water-Resistant Call Pendants because they were incorrectly programmed, which may prevent alarms from sounding when the button is pressed.

    Product
    Arial Wireless Water-Resistant Call Pendant The Arial Pendant tag is part of the Arial wireless emergency call management system. It enables residents in assisted living, skilled nursing or independent living to call staff with the press of a button.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0877-2013·2013-03-06

    Intel-GE Care Innovations Recalls QuietCare Facility Servers for Software Defect

    Intel-GE Care Innovations is recalling 19 QuietCare Facility Servers due to a software defect that may prevent Wander Alerts from being generated.

    Product
    QuietCare-Networked product, Facility Server/model: QC101601; The QuietCare system is intended to detect and analyze residents' movements.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·12701·2011-10-20

    ADT Recalls Carbon Monoxide Detectors for End-of-Life Signal Failure

    ADT is recalling about 20,000 hard-wired CO detectors that may fail to alert users when they reach the end of their useful life, posing a carbon monoxide poisoning hazard.

    Product
    CO 1224T Carbon Monoxide (CO) detectors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·00007a·1999-10-20

    Midland Weather Radios Recalled for Programming Error Affecting Alerts

    Midland Consumer Radio is recalling 9,000 weather radios due to a programming error that may prevent the device from recognizing certain National Weather Service signals.

    Product
    Midland weather radios
    Category
    Consumer Product
    Distribution
    Distributed nationwide