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.
Mitsubishi is recalling 2011-2015 Outlander Sport vehicles because water leaks can corrode the wiper motor, potentially causing loss of visibility and increasing crash risk.
Mitsubishi is recalling 2007-2013 Outlander vehicles because water intrusion can corrode the wiper link, potentially causing the wipers to stop working and reducing visibility.
Mazda is recalling 2010-2011 Tribute vehicles because a cracked fuel delivery module may leak fuel, increasing the risk of fire.
Jaguar is recalling 2017 F-Type SVR vehicles because rear suspension bolts may fail prematurely, potentially causing loss of vehicle control.
Vega Helmet Corporation is recalling specific XTA and XTA Touring half helmets because they may not adequately protect the wearer's head in a crash.
Forest River is recalling 92 model year 2017 Salem and Wildwood recreational trailers because the Federal Placard Label and VIN incorrectly state the vehicles have two axles instead of one.
Starcraft RV is recalling 94 model year 2017 AR-ONE trailers because incorrect Federal Placard and Cargo Carrying Capacity labels may lead to overloading and increased crash risk.
Con-Tech is recalling 2015-2017 BridgeKing concrete mixer trucks because fender mounts may crack, causing fenders to detach and create road hazards.
REV Recreation Group is recalling 2015-2016 Holiday Rambler Vacationer motorhomes because a front truss may not be adequately supported, risking wire or hydraulic line damage.
Peg Perego is recalling about 3,000 850 Polaris Sportsman ride-on vehicles because a circuit board defect can cause overheating, fire, and burns.
Forest River is recalling 2017 Vibe trailers because the kitchen stove may be connected to a live electrical circuit, posing a shock hazard.
Jayco is recalling 2017 Jay Sport camping trailers because tire labels list the wrong tire size and pressure, which could lead to over-inflation and tire failure.
QualiTech is recalling FE Bacon (Lot 31750) because a supplier reported the potential presence of E. coli O121 bacteria.
QualiTech, Inc. is recalling FE Spinach 352 due to a supplier notification regarding the potential presence of E. coli O121 bacteria.
Good Earth Egg Company is recalling shell eggs that may be contaminated with Salmonella. The product was distributed to customers in Georgia, Illinois, Kansas, and Missouri.
Kabobs Inc is recalling Mini Classic French Quiche because it was manufactured with flour contaminated with E. coli O121.
QualiTech is recalling FE Maple product code 27128 due to potential E. coli O121 bacteria. The product was distributed in ten US states and Canada.
Ford is recalling 2015-2017 Mustangs because an engine oil cooler hose may separate, causing an oil leak that could lead to engine failure or fire.
QualiTech is recalling FE Carrot 281 because a supplier notified them of potential E. coli O121 bacteria in the material.
QualiTech is recalling 3,200 lbs of FE Jalapeno 709 due to potential E. coli O121 contamination. The product was distributed in 10 US states and Canada.
Dollar General is recalling Soft Baked Chocolate Brownie Cookies due to the presence of mold. Consumers should discard the product or return it for a refund.
QualiTech is recalling FE Jalapeno 321A because a supplier reported the potential presence of E. coli O121 bacteria.
Windstone Medical Packaging is recalling 852 Major General Packs because Medtronic gloves inside may have splits or holes that compromise sterility.
Windstone Medical Packaging is recalling 115 Peri Kits (PSS1037) because the included Medtronic gloves may contain splits or holes that compromise sterility.
Vascular Solutions is recalling Twin-Pass RX Dual Access Catheters because excess manufacturing material may remain at the tip or within the distal lumen.