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.
Zimmer Biomet is recalling specific hip fracture stems because the internal patient label may be incorrect, although the outer box and product are correctly identified.
Zimmer Biomet is recalling specific femoral distal assemblies because the internal patient label may be incorrect, although the outer box and product are correctly identified.
Zimmer Biomet is recalling specific OSS Cemented IM Stem units because the internal patient label may be incorrect, although the outer box and product itself are correctly identified.
World Finer Foods is recalling Rapunzel Vegetable Bouillon because the front label claims no added salt, but sea salt is listed in the ingredients.
Zimmer Biomet is recalling CER BIOLOXD OPTION HD 32MM implants because the internal patient label may be incorrect, although the outer box and product are correctly identified.
Zimmer Biomet is recalling ECHO POR FMRL NC 9X125 medical devices because the internal patient label may be incorrect, although the outer box and product are correctly identified.
Zimmer Biomet is recalling a specific lot of distal femoral knee implant assemblies because the internal patient label may be incorrect, although the product itself is correctly identified.
Zimmer Biomet is recalling Lateral Troch Plate Full Crimp units because the internal patient label may be incorrect, though the product itself is correct.
Smiths Medical is recalling Medfusion Syringe Infusion Pumps because a loose clamp mechanism may cause the device to incorrectly alarm for invalid syringe sizes.
Zimmer Biomet is recalling CER OPTION TYPE 1 TPR SLEVE -6 devices because the internal patient label may be incorrect, although the outer box and product are correctly identified.
Zimmer Biomet is recalling Lateral Troch Plate Full Crimp devices because the internal patient label may be incorrect, although the outer box and product are correctly identified.
Zimmer Biomet is recalling COMP Primary Stem 8MM MINI devices because the internal patient label may be incorrect, although the product itself is correctly identified.
Beckman Coulter is recalling Access 2 Immunoassay Systems due to a potential for minor skin burns if the tool contacts the reagent storage interface board during pipettor alignment.
Beckman Coulter is recalling two UniCel DxC 600i SYNCHRON Access Clinical Systems because a tool may contact a board and cause minor skin burns during alignment.
Beckman Coulter is recalling three Access 2 Immunoassay Systems due to a potential risk of minor skin burns during pipettor alignment.
Hyundai is recalling 2006-2011 Azera and 2006 Sonata vehicles because water in the ABS module can cause an electrical short and engine fire.
Tesla is recalling 17,846 2013 Model S vehicles because the passenger frontal air bag inflators may explode during deployment, posing a risk of serious injury or death.
Chrysler is recalling specific 2009-2013 vehicles because the passenger air bag inflator may explode during deployment, posing a risk of serious injury or death.
Subaru is recalling 2009 Forester, Legacy, Impreza, Tribeca, WRX, and Outback vehicles because the passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
BMW is recalling 2007-2013 X5 and 2009-2013 X6 vehicles because the passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Mazda is recalling 2009 B-Series trucks because the passenger air bag inflator may explode during deployment, posing a risk of serious injury or death.
Mazda is recalling 2009-2013 CX-7, Mazda6, and CX-9 vehicles because the front passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Ferrari is recalling 1,899 2013 models because passenger air bag inflators may explode during deployment, potentially causing serious injury or death.
Subaru is recalling specific 2009-2013 models because passenger air bag inflators may explode during deployment, potentially causing serious injury or death.
Honda is recalling specific 2009-2013 Acura RL, Honda Element, and Ridgeline vehicles because the passenger air bag inflator may explode, posing a risk of serious injury or death.