Hazard

System Lockup recalls

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

What the numbers show

Total: 10
Critical: 0
Severe: 0
Most recent: 2021-09-29

Of the 10 system lockup 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.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all system lockup 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.

1–10 of 10

HighFDA (Devices)·Z-2484-2021·2021-09-29
Philips Affiniti Ultrasound Systems Recalled for Software Lock-Up During Exams
Philips Ultrasound is recalling Affiniti diagnostic ultrasound systems due to a software defect that intermittently causes device lock-ups when exiting Review Mode during patient exams. No illnesses or injuries have been reported.
Product
Affiniti Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and 5.0.2 Models: Affiniti 30 795121 Affiniti 30 795218 Affiniti 50 795208 Affiniti 50 795118 Affiniti 70 795210 Affiniti 70 795119
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1173-2021·2021-03-10
Siemens Sensis Vibe Systems Recalled for Potential System Freezes
Siemens is recalling 37 Sensis Vibe systems in the US because they may sporadically freeze during operation or idle, preventing user interaction.
Product
Sensis / Sensis Vibe systems with software version VD12 and equipped with HP Flex Pro-C PC. Diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies Model Numbers: Sensis Vibe Hemo 11007641 Sensis Vibe Combo 11007642 Sensis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1062-2017·2017-02-01
Philips Velara Generator Recall for System Lockup Risk
Philips is recalling 59 Velara Generators with old firmware used with the Integris BH5000 because the system may lock up.
Product
Velara Generator with an old Firmware version used with the Philips Integris BH5000
Category
Medical Device
Distribution
16 states
HighFDA (Devices)·Z-1061-2017·2017-02-01
Philips Recalls Velara Generators Due to Potential System Lockup
Philips is recalling 59 Velara Generators used with Allura Xper Systems because the devices may lock up. The recall is voluntary and covers units in the US and internationally.
Product
Velara Generator with an old Firmware version used with Philips Allura Xper Systems (Allura 15 & 12 (monoplane), Allura FD10C, Allura FD10F, Allura FD 10 F/C, Allura FD20, Allura XPER FD10/10, Allura XPER FD20 Biplane)
Category
Medical Device
Distribution
16 states
ModerateFDA (Devices)·Z-1572-2016·2016-05-04
Siemens ACUSON X700 Ultrasound System Recalled for Software Lockup
Siemens is recalling four ACUSON X700 ultrasound systems due to a software error that causes the system to lock up, requiring a reboot to recover operation.
Product
ACUSON X700 Ultrasound System with software version 1.0.04. Model numbers: 10658844 ACUSON X700 Ultrasound System 10658846 - ACUSON X700 Ultrasound System (Russia) 10658845 - ACUSON X700 Ultrasound System (Korea) Radiology: The Siemens ACUSON X700 ultrasound imaging syst
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-0853-2014·2014-02-05
GE Healthcare Recalls Innova IGS 630 Biplane Imaging Systems
GE Healthcare is recalling 28 Innova IGS 630 biplane imaging systems because a specific user action may cause the X-ray function to lock up.
Product
GE Healthcare Innova IGS 630. Biplane Cardiovascular and Interventional Imaging System. Product Usage: The angiographic X-ray systems are indicated for use for patients from newborn to geriatric in generating fluoroscopic and rotational images of human anatomy for cardiovascu
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0373-2014·2013-11-27
GE Vivid E9 Ultrasound Systems Recalled for Software Lockup
GE Healthcare is recalling 710 Vivid E9 ultrasound systems worldwide due to a software defect that can cause the system to slow down and lock up during critical procedures.
Product
GE Vivid E9 ultrasound system. GE Vivid E9 is a Track 3 diagnostic ultrasound system, which is primarily intended for cardiac imaging and analysis, but which also includes vascular and general radiology applications. The Vivid E9 incorporates a variety of electronic array trans
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2065-2012·2012-08-01
GE OEC 8800 Flexview X-ray System Recalled for Safety Issues
GE OEC Medical Systems is recalling OEC 8800 Flexview x-ray systems due to intermittent safety issues including navigation tracking inaccuracy and system lock-up.
Product
OEC 8800 Flexview, 892.1650 Image-intensified fluoroscopic x-ray system Product Usage: The 8800 Flexview is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical, and interventional procedures. Clinical applications may include c
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2040-2012·2012-08-01
GE OEC 6800 Miniview X-ray System Recalled for Safety Issues
GE OEC Medical Systems is recalling 1,933 OEC 6800 Miniview fluoroscopic x-ray systems due to intermittent safety issues, including navigation tracking inaccuracy and system lock-ups.
Product
OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremit
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1865-2012·2012-07-04
GE OEC Uroview 2800 Recalled for Intermittent Safety Issues
GE OEC Medical Systems is recalling 717 OEC Uroview 2800 fluoroscopic imaging systems due to intermittent safety issues, including navigation tracking inaccuracy and system lock-ups.
Product
OEC Uroview 2800, Model number A349855. Designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical, and interventional procedures.
Category
Medical Device
Distribution
0 states