State
73,722 recalls have nationwide distribution and so reach Georgia. 9,632 additional recalls listed Georgia specifically in their distribution scope.
Of the 9,632 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 2,565 (27%) are Severe.
Which agencies issued them
These figures cover only the 9,632 recalls whose distribution notice names Georgia specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
ArthroCare Corporation is voluntarily recalling 15,559 units of Smith&Nephew SmartStitch PerfectPasser Connectors because a manufacturing error may cause the upper jaw to detach during use.
LivaNova is recalling 77 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter during implantation.
Wright Medical Technology is recalling 16 Evolve Stem 8.5mm implants because they lack sterility assurance. The recall covers units distributed in the US and several international countries.
BMW is recalling certain 2020-2021 models due to debris in hybrid battery cells that could cause fire or injury. Owners are instructed not to charge vehicles or drive in manual mode.
GE Healthcare is recalling four NM/CT 860 SPECT/CT systems because rotor bearing screws were found loose on the detector.
Irvine Biomedical is recalling 40 units of Inquiry Steerable Diagnostic Catheters because packages were mislabeled with the wrong model and lot numbers, potentially causing procedure delays.
LivaNova is recalling 102 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter, preventing implantation.
Tesla is recalling 2020 Model Y vehicles with specific configurations because a software error prevents trailer brake lights from illuminating, increasing crash risk.
Perrigo is recalling 7.8 million Albuterol Sulfate inhalers nationwide because the delivery system may fail to dispense the medication.
Petzl is recalling approximately 14,850 low-stretch kernmantle ropes sold in the U.S. and Canada because deep cuts or tape securing rope ends can cause failure, posing fall and injury hazards.
Hologic is recalling 607 Panther Fusion Tube Trays because they may leak, potentially invalidating patient results or causing false negatives in flu and RSV assays.
Jayco is recalling 2021 Entegra motorhomes with Villa power seats because the electrical wiring may become damaged or chafed, causing short circuits and fire risk.
Suzuki is recalling 2018 GSX250R and GSX250RZ motorcycles because the headlight may fail, reducing visibility and increasing crash risk.
LivaNova is recalling specific lots of the Perceval Dual Collapser because complaints indicate the device may fail to collapse the heart valve during implantation.
LivaNova is recalling specific lots of Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter during implantation.
GE Healthcare is recalling 25 NM 830 detectors because rotor bearing screws were found loose. The devices are distributed in the US and internationally.
ArthroCare is recalling Speed Stitch Needle Cassettes because a supplier error may have resulted in needles made of titanium instead of stainless steel, posing a risk of breakage during use.
Bio-Rad is recalling BioPlex 2200 Syphilis Total & RPR kits because of increased RPR reactivity levels in the kit material.
GE Healthcare is recalling 15 NM/CT 870 CZT systems because rotor bearing screws were found loose on the detector.
GE Healthcare is recalling 31 NM/CT 870 DR systems because rotor bearing screws were found loose on the detector.
Preferred Pharmaceuticals is recalling specific lots of Nature-Throid tablets due to Current Good Manufacturing Practice (CGMP) deviations. The affected repackaged tablets were sold to three physicians in California and Georgia.
GE Healthcare is recalling nine Discovery NM670 Pro units because rotor bearing screws were found loose on the detector.
GE Healthcare is recalling 25 NM/CT 850 systems because rotor bearing screws were found loose on the detector.
Preferred Pharmaceuticals is voluntarily recalling Nature-Throid tablets due to CGMP deviations. The affected repackaged tablets were sold to three physicians in California and Georgia.
Irvine Biomedical is recalling 15 units of Inquiry Steerable Diagnostic Catheters because packages were mislabeled with the wrong model and batch numbers.