The Recall Desk

Hazard

Equipment Failure recalls

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

What the numbers show

Total
170
Critical
2
Severe
21
Most recent
2026-07-22

Of the 170 equipment failure recalls we have scored against our rubric, 2 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 21 (12%) 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 equipment 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.

151–170 of 170

  • HighFDA (Devices)·Z-1879-2013·2013-08-14

    Stryker Sonopet Ultrasonic Aspirator Console Recalled for Corrosion

    Stryker is recalling 215 Sonopet Ultrasonic Aspirator Consoles because corrosion on a power supply component may cause the irrigation pump to stop working.

    Product
    Sonopet Ultrasonic Aspirator Console 5450-851-000(Console 100V) Product Usage: The Sonopet Console is indicated for use in surgical procedures where fragmentation, emulsification, and aspiration of soft and hard tissue is desirable, including neurosurgery, gastrointestinal
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1750-2013·2013-07-24

    Siemens AXIOM Artis zee/zeego Systems Recalled for Generator Power Supply Defect

    Siemens is recalling 23 AXIOM Artis zee/zeego angiographic x-ray systems because a tolerance problem in the generator power supply may cause the generator to fail.

    Product
    Siemens AXIOM Artis zee/zeego systems equipped with generator A100 Plus Product Usage: Angiographic x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1318-2013·2013-05-22

    GE Healthcare Recalls Innova Fluoroscopic Systems Due to Relay Failure

    GE Healthcare is recalling 713 Innova fluoroscopic systems because a relay failure in the power distribution box can cause sudden loss of imaging modes without warning.

    Product
    GE Healthcare Innova 2100 IQ, Innova 3100 IQ, Innova 4100 IQ, Innova 2121 IQ, Innova 3131 IQ , Innova 3100, Innova 4100. For use in generating fluoroscopic images of human anatomy for diagnostic and interventional procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0271-2013·2012-11-14

    Sorin S5 Perfusion System Recalled for Motor Controller Faults

    Sorin Group USA is recalling S5 Perfusion Systems due to motor controller faults that may cause unintended pump stoppage during surgery.

    Product
    S5 Single Roller Pump 150, Item Number: 10-80-00 The Stockert S5/Sorin C5 System is intended to be used during cardiopulmonary bypass for procedures lasting six hours or less.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0274-2013·2012-11-14

    Sorin S5 Perfusion System Recalled for Motor Controller Faults

    Sorin Group USA is recalling S5 Perfusion Systems due to a motor controller fault that could cause unintended pump stoppage during surgery.

    Product
    S5 Mast Roller Pump 150, Item Number: 10-88-00 The Stockert S5/Sorin C5 System is intended to be used during cardiopulmonary bypass for procedures lasting six hours or less.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2178-2012·2012-08-15

    Terumo Advanced Perfusion System 1 recalled for module malfunctions

    Terumo is recalling 649 Advanced Perfusion System 1 units worldwide due to faulty components in the Occluder and Air Bubble Detection modules.

    Product
    System 1 base 220/240V The Terumo Advanced Perfusion System 1 is indicated for use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures only when used by a qualified perfusionist who is experienced in the oper
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2132-2012·2012-08-08

    Baxter Recalls Peritoneal Dialysis Solution Due to Incorrect Inspection Instructions

    Baxter Healthcare is recalling Extraneal and DIANEAL Low Calcium peritoneal dialysis solutions because a technical service representative provided incorrect instructions for inspecting solution bags.

    Product
    Extraneal and/or DIANEAL LOW CALCIUM Peritoneal Dialysis Solution in Plastic Container, PL-146 used with Automated Peritoneal Dialysis System/Automated PD Set with Cassette; Manufactured for Baxter Healthcare Corporation, Deerfield, IL 60015 U.S.A. The HomeChoice dialysis system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2027-2012·2012-07-25

    GE OEC 8800 Flexiview Imaging Device Recall for Defective Power Supply

    GE OEC Medical Systems is recalling OEC 8800 Flexiview imaging devices because an FDA inspection found a defective vertical lift column power supply subject to early life failure.

    Product
    OEC 8800 Flexiview designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. The OEC 8800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventio
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1968-2012·2012-07-18

    Terumo Advanced Perfusion System 1 Recalled for Roller Pump Occlusion Malfunctions

    Terumo CVS is recalling 992 units of the Advanced Perfusion System 1 due to roller pump occlusion malfunctions that could prevent pump use.

    Product
    System 1 Base 100/120V The Terumo Advanced Perfusion System 1 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a qualified medical professional who
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1900-2012·2012-07-11

    CareFusion AirLife Infant Breathing Circuits Recalled for Cracking Adapter

    CareFusion is recalling AirLife infant breathing circuits because a Y adapter may crack, causing a leak that reduces air delivery to ventilated patients.

    Product
    AirLife Isothermal Breathing Circuit, Infant Respiratory Circuit, Non-Heated; an Rx device for single patient use; CareFusion, 22745 Savi Ranch Parkway, Yorba Linda, CA 92887 USA, Made in Mexico Respiratory breathing circuits are used with a ventilator when mechanical ventilat
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·10197·2010-04-14

    Mares Nemo Air Dive Computers Recalled Due to Drowning Hazard

    Mares is recalling Nemo Air dive computers because a failing O-ring can cause a slow loss of breathing gas, posing a drowning risk to divers.

    Product
    Mares Nemo Air Dive Computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·08393·2008-09-10

    Aqua Lung Recalls Scuba Regulators and Adapters Due to Drowning Hazard

    Aqua Lung is recalling Titan DIN scuba regulators and adapters because a broken retainer can cause rapid air loss and regulator detachment, posing a drowning risk.

    Product
    Titan DIN 1st Stage Scuba Regulators and Titan/Conshelf DIN Scuba Adaptors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·08139·2007-12-18

    Gorilla Recalls Full Body Safety Harnesses Due to Fall Hazard

    Gorilla is recalling about 60,000 full body safety harnesses because they could fail during use, posing a risk of serious injury or death.

    Product
    Full Body Safety Harnesses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·07501·2006-10-02

    Scubapro MK 20 Scuba Regulators Recalled for Service Upgrade

    Scubapro is recalling about 48,500 MK 20 first stage regulators because over-tightening during service could cause failure and drowning. Consumers should have the unit serviced for free.

    Product
    Scubapro® MK 20 First Stage Regulators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·77131·1977-12-27

    CPSC Recalls 2,000 Poseidon Cyklon 300 Scuba Regulators for Hose Defect

    CPSC and Parkway Fabricators are replacing intermediate air hoses on 2,000 Poseidon Cyklon 300 scuba regulators due to a defect that may cause air flow to stop.

    Product
    Scuba Regulators Replaced by Parkway Fabricators
    Category
    Consumer Product
    Distribution
    Distributed nationwide