State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mercedes-Benz is recalling 2016-2017 AMG GLE43 vehicles because software conflicts may cause the engine to shut down while driving, increasing crash risk.
Navistar is recalling 2018 International LT and HX trucks because a fuel pump gear may slip, causing engine stalls that increase crash risk.
KME is recalling 2012-2017 Predator Aerial vehicles because a software error may cause the ladder to accelerate unexpectedly, increasing injury risk.
KME is recalling 2014-2016 Predator Aerial and Predator SS Aerial vehicles because ladder rotation software may allow unintended movement, increasing injury risk.
Ride the Ducks is recalling 1996-2005 amphibious vehicles because the front axle housing may fracture, potentially causing a loss of vehicle control.
Forest River is recalling 2016-2017 Berkshire vehicles because an improperly installed battery cable bracket may cause chafing and short circuits, increasing fire risk.
Streetcar ORV LLC is recalling 2013-2017 RAM 2500 and 3500 trucks modified with specific cast aluminum wheels that may fracture, causing rapid air loss and potential loss of vehicle control.
Temsa is recalling 2014-2018 TS45 coach buses because the tag axle steering hydraulic hose may leak or burst, potentially causing loss of control or fire.
Kawasaki is recalling approximately 15,000 KFX50 and KFX90 all-terrain vehicles because a leaking fuel tap poses a fire hazard. No injuries have been reported.
Clif Bar & Company is recalling Clif Builders Chocolate Mint bars due to undeclared peanuts and/or tree nuts. The recall covers multiple pack sizes distributed nationwide and internationally.
Clif Bar & Company is recalling Clif Kid Zbar Protein Chocolate Chip bars due to undeclared peanuts and/or tree nuts.
Clif Bar & Company is recalling Clif Builders Variety Packs due to undeclared peanuts and/or tree nuts.
Clif Bar & Company is recalling Clif Kid Zbar Protein Variety Packs due to undeclared peanuts and/or tree nuts.
Vi-Jon, Inc. is recalling 101,244 bottles of Magnesium Citrate Oral Solution because the product was found to contain mold identified as Rhinocladiella similis.
Newmar is recalling 2014-2017 Dutch Star and 2014 Mountain Aire recreational vehicles because a battery cable may short circuit, increasing the risk of a fire.
Clif Bar & Company is recalling Clif Kid Zbar Protein Chocolate Mint bars due to undeclared peanuts and/or tree nuts.
LivaNova is recalling Perfusion Tube Sets because included Medtronic display sets may have packaging pinholes, creating a risk of sterile barrier breach.
LivaNova is recalling Perfusion Tube Sets because included Medtronic display sets may have packaging pinholes that compromise sterility.
LivaNova is recalling Perfusion Tube Sets because included Medtronic display sets may have packaging pinholes, creating a potential sterile barrier breach.
Hologic is recalling 164 Tomcat Instruments due to a software anomaly that may cause the pipettor arm to contact the mucous shelf, potentially leading to incorrect patient results.
LivaNova is recalling Perfusion Tube Sets because included Medtronic display sets may have packaging pinholes, creating a potential sterile barrier breach.
LivaNova is recalling Perfusion Tube Sets because included display sets may have packaging pinholes that compromise sterility.
LivaNova is recalling Perfusion Tube Sets because they may contain Medtronic display sets with packaging pinholes that could breach the sterile barrier.
LivaNova is recalling Perfusion Tube Sets because included Medtronic display sets may have packaging pinholes, creating a risk of sterile barrier breach.
LivaNova is recalling Perfusion Tube Sets because included Medtronic display sets may have pinholes in their packaging, creating a potential sterile barrier breach.