Hazard

Gas Release recalls

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

What the numbers show

Total: 11
Critical: 0
Severe: 1
Most recent: 2021-09-01

Of the 11 gas release 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 (9%) 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 gas release 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.

1–11 of 11

HighFDA (Devices)·Z-2342-2021·2021-09-01
Philips Ingenia MRI System recalled due to incorrect pressure relief valve
Philips recalled 27 units of the Ingenia 1.5T Magnetic Resonance system with an incorrect pressure relief valve (42 psi instead of 3.75 psi) that could release helium gas and cause injury.
Product
Ingenia 1.5T-Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body or extremities Model Number: 7
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1433-2018·2018-04-25
Philips Intera 1.5T MRI Systems Recalled for Helium Gas Risk
Philips is recalling Intera 1.5T MRI systems due to a potential risk of helium gas release during a magnet quench.
Product
Intera 1.5T; 1) Intera 1.5T Omni/Stellar Model 781104, 2) Intera 1.5T Power/Pulsar Model 781105, 3) Intera 1.5T Master/Nova Model 781106, 4) Intera 1.5T Master CV Model 781107, 5) Intera 1.5T Explorer/ Nova Dual Model 781108, 6) Intera 1.5T IT Model 781160, 7) Intera 1.5T Pulsa
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1434-2018·2018-04-25
Philips Panorama 1.0T MRI Recalled for Helium Gas Release Risk
Philips is recalling Panorama 1.0T MRI scanners due to a potential risk of helium gas release into the examination room during a magnet quench.
Product
Panorama 1.0T, Model 781250 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1441-2018·2018-04-25
Philips Multiva MRI Systems Recalled for Helium Gas Quench Risk
Philips is recalling 8,205 Multiva MRI systems worldwide due to a potential risk of helium gas release during a magnet quench.
Product
Multiva systems; 1) Magnets Multiva 16 Model 781487, 2) Magnets 8 Model 781488, 3) Magnet Achieva 1.5T, Model 781492, 4) Magnet HFO, Model 781495, 5) Magnet Multiva 16, Model 781496, 6) Magnet Multiva 8, Model 781497 & 7) Magnets Ingenia 1.5T CX, Model 781498 Product Usage:
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1431-2018·2018-04-25
Philips Intera 0.5T MRI Recalled for Helium Gas Risk
Philips is recalling 8,205 Intera 0.5T MRI scanners worldwide due to a potential risk of helium gas release during a magnet quench.
Product
Intera 0.5T Standard, Model 781101 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1432-2018·2018-04-25
Philips Intera 1.0T MRI Systems Recalled for Helium Gas Risk
Philips is recalling 8,205 Intera 1.0T MRI systems worldwide due to a potential risk of helium gas release during a magnet quench.
Product
Intera 1.0T; 1) Stellar Model 781102, 2) Pular Model 781103 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1442-2018·2018-04-25
Philips T5 MRI Scanner Recalled for Helium Gas Risk
Philips is recalling T5 MRI scanners due to a potential risk of helium gas release during a magnet quench.
Product
T5 Model 78104 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1438-2018·2018-04-25
Philips T5-NT MRI Scanner Recalled for Helium Gas Risk
Philips is recalling 8,205 T5-NT MRI scanners worldwide due to a potential risk of helium gas release in the examination room during a magnet quench.
Product
T5-NT, Model 78104 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1430-2018·2018-04-25
Philips Multiva MRI Systems Recalled for Helium Gas Risk During Quench
Philips is recalling 8,205 Multiva MRI systems worldwide due to a potential risk of helium gas release in the examination room during a magnet quench.
Product
Multiva systems, 1) Multiva 1.5T 8 R5 Model 781072, 2) Multiva 1.5T 16 R5 Model 781073, 3) Multiva 1.5T 8ch R5 based Model 781074, 4) Multiva 1.5T Model 781076, & 5) Multiva 1.5T 16ch R5 based Model 781078 Product Usage: Indicated for use as a diagnostic device. It can produ
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1440-2018·2018-04-25
Philips T10-NT MRI Systems Recalled for Helium Gas Risk
Philips is recalling 8,205 T10-NT MRI systems due to a potential risk of helium gas release in the examination room during a magnet quench.
Product
T10-NT, Model 78107 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·15V816000·2015-12-07
Freightliner Cascadia CNG Vehicles Recalled for Exhaust Fire Risk
Daimler Trucks North America is recalling 2013-2015 Freightliner Cascadia CNG vehicles because hot exhaust near the pressure relief device may cause gas release and fire.
Product
FREIGHTLINER — FREIGHTLINER CASCADIA
Category
Vehicle
Distribution
Distributed nationwide