State
73,809 recalls have nationwide distribution and so reach Georgia. 9,635 additional recalls listed Georgia specifically in their distribution scope.
Of the 9,635 recalls naming Georgia we have scored against our rubric, 1,471 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,567 (27%) are Severe.
Which agencies issued them
These figures cover only the 9,635 recalls whose distribution notice names Georgia 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 sterile Jamshidi bone marrow needles because the integrity of the sterile packaging is potentially compromised.
Midwest Northern Inc. is recalling Buffalo Style Peanuts due to potential allergen cross-contact in the roasting oil.
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.
Midwest Northern Inc. is recalling Nut Criss Cross Mix trail mix due to potential allergen cross-contact in the oil used to roast nuts and seeds.
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.
Midwest Northern Inc. is recalling roasted salted almonds due to potential allergen cross-contact in the roasting oil.
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.
Midwest Northern Inc. is recalling Sizzlin' Sweet Snack Mix due to potential allergen cross-contact in the oil used to roast nuts and seeds.
Midwest Northern Inc. is recalling Cajun Peanuts due to potential allergen cross-contact in the roasting oil. Consumers should check lot numbers and stop eating the product.
Midwest Northern Inc. is recalling Spanish Peanuts due to potential allergen cross-contact in the roasting oil. The recall affects 35,056 lbs distributed to 13 states.
Midwest Northern Inc. is recalling roasted salted pumpkin seeds due to potential allergen cross-contact in the roasting oil.
Midwest Northern Inc. is recalling 5-pound bags of Backwoods Trail Mix due to potential allergen cross-contact in the oil used to roast the nuts and seeds.
Siemens is recalling 15 Oncor Impression Plus linear accelerators to update software and reduce the risk of collision during automated cancer treatments.
Midwest Northern Inc. is recalling specific lots of Food Service Trail Mix due to potential allergen cross-contact in the oil used to roast nuts and seeds.
Midwest Northern Inc. is recalling 5 lb. bags of Roasted & Salted Nut Mix due to potential allergen cross-contact in the roasting oil.
Midwest Northern Inc. is recalling 35,056 lbs of Nut Cinnamon Apple Mix due to potential allergen cross-contact in the oil used to roast nuts and seeds.
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.