State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Siemens is recalling 13 SOMATOM Perspective CT systems to replace a component that could cause power cutouts during use.
GE Healthcare is recalling Prestige VH and other medical systems because aged CRT monitors may fall.
Curio Design is recalling Splyt modular light kits and bases because cracked pieces and faulty wires pose shock and fire hazards. No injuries have been reported.
GE Healthcare is recalling Legacy and other imaging systems because aged CRT monitors may fall. The recall covers 1,598 units distributed in the US and internationally.
GE Healthcare is recalling Prestige SI and other systems because aged CRT monitors may fall. The recall covers 1,598 units in the US and overseas.
PerkinElmer Health Sciences is recalling 21 units of Specimen Gate Laboratory and eReports software because a defect may cause excessive disk space consumption, leading to software failure.
Bio-Botanica is recalling Nature's Answer and Seeking Health Vitamin D-3 drops because the lots contain more Vitamin D3 than the label claims.
Virtus Pharmaceuticals is recalling Virt-Select Prenatal/Postnatal Softgels because the active ingredient manufacturer is on an FDA Import Alert for cGMP deviations.
Ortho-Clinical Diagnostics is recalling VITROS Intact PTH Reagent Packs due to a positive bias of up to 20% and an incorrectly set reference interval.
Shimadzu Medical Systems is recalling 39 SONIALVISION G4 X-ray TV Systems due to a potential oil leak from the x-ray tube housing.
Virtus Pharmaceuticals is recalling VirtPrex Prenatal/Postnatal Tablets because the active ingredient manufacturer is on an FDA Import Alert.
Care-Tech Laboratories is recalling Techni-Care Surgical Hand Scrub because bottles have missing or illegible lot and expiration dates, as well as defective or cracked caps.
Virtus Pharmaceuticals is recalling 2,406 bottles of Extra-Virt Plus DHA Prenatal/Postnatal Softgels because the API manufacturer is on FDA Import Alert.
Virtus Pharmaceuticals is recalling Virt-Advance Prenatal/Postnatal Softgels because the active ingredient manufacturer is on an FDA Import Alert.
Takata is recalling certain frontal passenger air bag inflators that may rupture due to propellant degradation, posing a risk of serious injury or death.
Takata is recalling specific frontal passenger air bag inflators in 2012 vehicles registered in 14 states and territories due to a risk of rupture.
Volkswagen Group of America is recalling specific Audi models because a blocked coolant pump can overheat and cause a fire.
REV is recalling 2017 Fleetwood and Holiday Rambler motor homes because the rear sway bar may detach, increasing crash risk.
Volkswagen Group of America is recalling 2011-2017 Audi Q5 vehicles because water in the sunroof drainage system may corrode side air bag inflators, posing a risk of serious injury.
Sumitomo is recalling specific Kelly Armorsteel KDA tires manufactured in December 2016 because they lack required safety markings on the sidewalls.
Forest River is recalling 2017 XLR Toyhauler and Prime Time Spartan fifth-wheel vehicles because rear cargo door hinge welds may be insufficient, increasing the risk of personal injury.
BMW is recalling specific 2016-2017 S 1000 RR and S 1000 R motorcycles because a rear suspension bolt may loosen, affecting handling and increasing crash risk.
Porsche is recalling 2017 911, 718 Cayman, and 718 Boxster vehicles because the side air bag inflator initiator may fail to ignite during a crash.
Hyundai is recalling 2017 Sonata and Elantra vehicles because the driver's air bag inflator seal may be improperly installed, potentially reducing protection in a crash.
4moms is recalling specific Self Installing Rear-facing Infant Car Seats because a tight rivet may prevent the carrier from securely attaching to the base, increasing injury risk in a crash.