State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Keystone is recalling 2020 Cougar 30RKD trailers because emergency exit windows lack red handles and labels, potentially delaying evacuation during an emergency.
Siemens Medical Solutions is recalling syngo.CT software version VA48A_SP5.5 for specific SOMATOM CT models due to scanning workflow interruptions and unexpected user notifications.
B. Braun Medical is recalling 200 units of Accu-Bloc Perifix Kits because damaged filter membranes may prevent the device from achieving required filter capacity.
Integra LifeSciences Corp. is recalling 237 units of the Jarit GEMINI CLAMP because a small crack may cause corrosion and breakage after repeated sterilization.
Cincinnati Sub-Zero Products LLC is recalling Norm-O-Temp model 111Z devices because the manual lacks instructions warning that exceeding 40 Celsius for extended periods can cause tissue damage.
Ford is recalling 2017 Ford Explorer vehicles with power front seats because the seat frames may have sharp edges that could injure occupants.
B. Braun Medical is recalling 540 units of CE17TKN epidural Tuohy needle filters because the filter membrane is damaged, preventing the device from achieving its intended filter capacity.
B. Braun Medical is recalling 200 units of Con Epi Trays because damage to the filter membrane prevents the device from achieving its required filter capacity.
B. Braun Medical is recalling 3,820 units of Accu-Bloc Perifix Kits because damage to the filter membrane prevents the device from achieving its intended filter capacity.
B. Braun Medical is recalling 200 units of spinal and epidural trays because the filter membrane is damaged, preventing the device from achieving required filter capacity.
Heidelberg Engineering is recalling 29 SPECTRALIS ophthalmic imaging devices because a software configuration error may cause incorrect display of patient master data.
Fujifilm is recalling 174 FDR Go Plus mobile X-ray systems because a graphics driver issue may cause the device to display a Blue Screen of Death.
Roche is recalling Tina-Quant Myoglobin Gen. 2 assays due to signal drops causing calibration failures and QC imprecision on specific analyzers.
Coltene is recalling a specific lot of Diatech diamond dental burs because the instruments in the batch vary in length despite having the same shape and grit.
Alere San Diego, Inc. is recalling 186 Alere Cholestech LDX Analyzer kits because the power supplies have reversed polarity, rendering the devices inoperable.
Getinge is recalling 1,444 boxes of disposable CO2 absorbers because the expiration and manufacturing dates on the labels are reversed.
Ragdoll & Rockets is recalling about 14,100 units of children's loungewear because the items fail to meet federal flammability standards for sleepwear, posing a risk of burn injuries.
Healing Solutions is recalling Wintergreen and Birch essential oils because the bottles lack required child-resistant caps, posing a poisoning risk to young children.
E-One is recalling one 2018 Typhoon emergency vehicle because the foam pump system can overheat and fail, making firefighting foam unavailable.
DIANA is recalling Stormrider Gen 2 air rifles because they can unexpectedly discharge even when the safety is engaged, posing a risk of serious injury or death.
Isuzu is recalling 2017-2019 N-Series and Chevrolet Low Cab Forward trucks because a loose bolt in the relay box may cause electrical failure and vehicle stalling.
Mercedes-Benz is recalling 2020 GLE 350 and GLE 450 vehicles because the owner's manuals lack instructions for adjusting third-row head restraints, violating federal safety standards.
TAP Worldwide is recalling 840 Pro Comp Extended Thread lug nuts that may be incorrectly sized. The defect could prevent proper tightening, leading to lug stud failure and increased crash risk.
General Motors is recalling 2020 Buick Enclave and Chevrolet Traverse vehicles because a crack in the right-hand frame rail may reduce crash performance and increase injury risk.
General Motors is recalling 2014-2018 Chevrolet, GMC, and Cadillac vehicles because a vacuum pump defect may reduce brake assist, increasing stopping distance.