State
73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ducati is recalling 2017-2019 Supersport motorcycles because vibrations may distort mirror images, reducing rearward visibility and increasing crash risk.
Keystone is recalling 2018-2019 Raptor recreational trailers because tires may rub against the frame, potentially affecting handling and increasing crash risk.
Honda is recalling 2018-2019 Odyssey vehicles because power sliding door latches may stick and fail to latch, potentially allowing doors to open while driving.
A. O. Smith is recalling approximately 616,000 gas water heaters because a torn burner screen can cause excess heat and fire if installed on combustible floors.
Honda is recalling approximately 56,000 Pioneer 1000 recreational off-highway vehicles because an incorrectly installed throttle body can ignite, posing fire and burn hazards.
H.I.S. is recalling Self-Esteem brand girl's clothing sets because the included pendant necklaces contain lead levels exceeding federal bans. No injuries have been reported.
Mountain Warehouse is recalling about 1,000 children's water bottles because the spout can detach, creating a choking hazard. No injuries have been reported.
Chrysler is recalling 2018 Jeep Wrangler four-door vehicles because the right rear door latch may be misaligned, potentially preventing the door from latching properly.
A. O. Smith is recalling specific 30-gallon gas water heaters sold at Lowe's in California because the flame arrestor may fail, posing a fire risk.
Lifetone Technology is recalling HLAC151 Bedside Fire Alarm and Clocks because the optional bed shaker may fail to operate during a fire emergency.
Silverstone is recalling Ride Eazy DOT Sleek helmets because they may not adequately protect wearers in a crash, increasing injury risk.
Pharm D Solutions is recalling Caffeine and Sodium Benzoate Injection 125 mg/125 mg/mL due to a lack of assurance of sterility. The recall covers 567 milliliters distributed nationwide.
Pharm D Solutions is recalling Bi-Mix Injection due to a lack of assurance of sterility. The product was distributed nationwide.
Dexter Axle Company is recalling specific trailer axles because inner hub bearings may lack sufficient grease, risking overheating and failure.
Pharm D Solutions is recalling Trimix BM3 Papaverine 30 mg/Phentolamine 1 mg Injectable because the agency could not ensure the product was sterile.
Pharm D Solutions is recalling 29 bottles of Calcium Gluconate 1% Eyewash because the company cannot ensure the product is sterile.
Pharm D Solutions is recalling 179 vials of Sermorelin/Ipamorelin powder because the company cannot ensure the product is sterile.
Pharm D Solutions is recalling 420 vials of Sermorelin/GHRP-2/GHRP-6 powder nationwide due to a lack of assurance of sterility.
Pharm D Solutions is recalling specific lots of Trimix T-106 aqueous solution because the company cannot ensure the product is sterile.
Avella of Deer Valley is recalling 1,360 bags of Morphine in NS due to a lack of assurance of sterility. The product was distributed nationwide.
Siemens is recalling 35 Multix Fusion radiographic systems because steel cables in the lifting column may rupture without triggering the safety lock, causing the arm to drop unexpectedly.
Pharm D Solutions is recalling 881 vials of HCG Lyopholized 1200 IU Injectable nationwide due to a lack of assurance of sterility.
Siemens is recalling 142 Ysio radiographic systems because steel cables may rupture, causing the tube arm to drop unexpectedly during patient positioning.
Pharm D Solutions is recalling Ascorbic Acid 500 mg/mL Solution due to a lack of assurance of sterility. The recall affects nationwide distribution.
Pharm D Solutions is recalling 765 vials of HCG 3000 Unit Powder nationwide due to a lack of assurance of sterility.