State
73,809 recalls have nationwide distribution and so reach South Carolina. 7,153 additional recalls listed South Carolina specifically in their distribution scope.
Of the 7,153 recalls naming South Carolina we have scored against our rubric, 1,275 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,170 (30%) are Severe.
Which agencies issued them
These figures cover only the 7,153 recalls whose distribution notice names South Carolina specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Carefusion 2200 Inc is recalling 4,240 units of sterile manometers because the integrity of the sterile packaging is potentially compromised.
Philips is recalling 291 Brilliance 64 CT scanners because a software defect prevents Surview scans from initializing when tube current is below 30 mA.
Philips is recalling 151 Ingenuity Flex CT scanners because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient loading.
Getinge is recalling 170 automated loading/unloading systems for Washer-Disinfector 88 Series units. The recall addresses a risk that disinfected goods may fall to the floor if the trolley is not docked.
Siemens is recalling one Oncor Avant-garde linear accelerator to update software and reduce the risk of collision during automated cancer treatments.
Carefusion 2200 Inc is recalling sterile Jamshidi bone marrow needles because the integrity of the sterile packaging is potentially compromised.
Cook Inc. is recalling 483 MINC Benchtop Incubators because a heater failure may cause temperatures to become too high or too low for proper cell culture.
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.
Philips Medical Systems is recalling six Brilliance 64 CT systems because closing the emergency stop may disable the horizontal motor, allowing the couch to move during patient loading.
Philips is recalling Intera 1.5T MRI systems due to a potential risk of helium gas release during a magnet quench.
Cook Inc. is recalling 4,451 MINC Benchtop Incubators because a heater defect may cause temperatures to become too high or too low for proper cell culture.
Philips is recalling 47 IQon Spectral CT systems because closing the emergency stop may disable the horizontal motor, allowing the couch to move during patient loading.
Siemens is recalling 15 Oncor Impression Plus linear accelerators to update software and reduce the risk of collision during automated cancer treatments.
Stryker is recalling 4,724 Power-LOAD Cot Fastening Systems because the floor plates holding ambulance cot anchors may be broken.
Philips is recalling 106 Brilliance Big Bore CT scanners because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient loading or unloading.
Siemens is recalling 18 PRIMUS HI Digital Linear Accelerators to update software and reduce the risk of collision during automated cancer treatments.
Philips is recalling 8,205 Intera 0.5T MRI scanners worldwide due to a potential risk of helium gas release during a magnet quench.
Philips is recalling 281 Ingenuity Core CT systems because the emergency stop may fail to lock the couch, allowing it to move during patient loading.
Zimmer Biomet is recalling specific proximal femoral components due to potential machining debris that may not have been adequately removed during cleaning.
Siemens is recalling 18 MEVATRON M2 linear accelerators to update software and reduce the risk of collision during automated cancer treatments.
Philips is recalling T5 MRI scanners due to a potential risk of helium gas release during a magnet quench.
Halyard Health is recalling certain Closed Suction Systems because Flex Connectors may become loose or disconnect before or during use.
HD Supply is recalling Seasons ceiling fans because brackets can break, causing blades to fall. No injuries have been reported, but one instance of minor property damage occurred.
Siemens is recalling seven ONCOR Impression Digital Linear Accelerators to update software and reduce the risk of collision during automated cancer treatments.
Philips is recalling 8,205 Achieva 1.5T MRI systems worldwide due to a potential risk of helium gas release during a magnet quench.