Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Autochair is recalling Milford Smartbase units because a weak spring and misaligned locking pin caused legs to fold, dropping a person.
Philips is recalling 19 Brilliance iCT SP CT systems because closing the emergency stop may disable the horizontal motor, allowing the couch to move during patient loading.
Cook Inc. is recalling 132 Cook Vacuum Pumps (K-MAR-5200-US) worldwide due to defective crimp connectors that may cause device failure, electric shock, or burns.
Cook Inc. is recalling 2,267 Cook Vacuum Pumps (K-MAR-5200-US) worldwide due to defective crimp connectors that may cause device failure, electric shock, or burns.
Philips is recalling 119 Brilliance Big Bore CT systems because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient load or unload.
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.
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.
Draeger Medical Systems is recalling Infinity Acute Care System monitoring solutions because invasive pressure alarms may not activate.
Getinge is recalling 170 automated loading/unloading accessories for Washer-Disinfector 86 Series units due to a risk of disinfected goods falling to the floor.
Carefusion 2200 Inc is recalling 1,200 sterile thoracentesis and paracentesis kits because their packaging integrity may be compromised.
Life Technologies is recalling three lots of Human Fetal Hemoglobin FITC Conjugate because high background and unusual staining may cause false positive results.
Philips is recalling Ingenia 1.5T CX MRI scanners due to a potential risk of helium gas release into the examination room during a magnet quench.
Philips is recalling the SmarthPath to dStream conversion software for 1.5T MRI systems due to a potential risk of helium gas release during a magnet quench.
Philips is recalling Brilliance 6 Slice CT systems because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient loading.
NeuroLogica Corporation is recalling 16 solid state x-ray imagers because the retrofit equipment poses a potential foot injury risk during backward transport.
Philips is recalling 8,205 Multiva MRI systems worldwide due to a potential risk of helium gas release during a magnet quench.
Philips is recalling 8,205 Intera 1.0T MRI systems worldwide due to a potential risk of helium gas release during a magnet quench.
Philips is recalling 172 Ingenuity CT systems because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient load or unload.
Philips is recalling two Brilliance 16 Slice CT systems because the emergency stop may fail to disable the horizontal motor, allowing the couch to move during patient loading.
Carefusion 2200 Inc is recalling 14,200 Jamshidi (TJ) needles because the integrity of the sterile packaging is potentially compromised.
Tornier, Inc. is recalling 32,253 units of Phantom Fiber sutures because improper storage may cause the raw material to degrade, leading to a loss of suture strength.
Halyard Health is recalling certain Closed Suction Systems because the Flex Connectors may become loose or disconnect before or during use.
Carefusion 2200 Inc is recalling specific lots of Illinois needle aspiration devices because their sterile packaging integrity is potentially compromised.
Philips is recalling 591 Ingenuity Core 128 CT systems because closing the emergency stop may allow the patient couch to move during loading or unloading.
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.