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.
Jayco is recalling 2019 Jay Flight SLX, Jay Feather, and White Hawk travel trailers because inner wheel hub bearings may lack sufficient grease, risking overheating and hub failure.
Mercedes-Benz is recalling specific 2015-2019 models because a steering rack locknut may break, causing the steering to stick and increasing crash risk.
Mercedes-Benz is recalling 2019 E450 and E63S Wagons because the tailgate spoiler may detach while driving, creating a road hazard.
Daimler Vans USA is recalling 2016-2017 Mercedes-Benz Metris vehicles because a fuel hose may leak, increasing the risk of a fire.
Horizon Global is recalling specific Reese Elite Aftermarket Gooseball kits installed on Chevrolet and GMC trucks due to a risk of trailer separation.
Sciegen Pharmaceuticals is recalling Irbesartan 300mg tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA).
Sciegen Pharmaceuticals is recalling GSMS Irbesartan Tablets, 75 mg, because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).
Altec is recalling 2017 AT37, AT41, and AT48 aerial devices because loose or missing fasteners may cause the pedestal to separate, increasing injury risk.
Beckman Coulter is recalling Cytomics FC 500 and EPICS XL flow cytometers due to a manufacturing defect on the amplifier board that may cause signal loss or drifting.
Sciegen Pharmaceuticals is recalling GSMS Irbesartan Tablets, 150 mg, because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).
Beckman Coulter is recalling 2,549 flow cytometers worldwide due to a manufacturing defect that may cause signal loss or drifting, potentially affecting patient results.
Ford is recalling 2016-2018 Focus vehicles with 1.0L engines and manual transmissions because a clutch fracture could cause a fluid leak and fire risk.
Smiths Medical is recalling 10,440 Irrisept OR bottle assemblies because leaking containers may compromise sterility, posing an infection risk.
Sciegen Pharmaceuticals is recalling GSMS Irbesartan Tablets, USP, 300 mg, because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).
TSE Brakes is recalling specific Air Brake Actuators because mounting washers may fracture, potentially reducing braking ability and increasing crash risk.
Porsche is recalling 2018 Panamera Hybrid models because front brake lines may corrode, potentially reducing braking performance and increasing crash risk.
Sciegen Pharmaceuticals is recalling Westminister Irbesartan Tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA).
Keystone RV Company is recalling certain 2019 recreational trailers because the inner axle hub bearings may not have been sufficiently greased, which could cause overheating, hub failure, and increased crash risk.
Blue Bird is recalling certain 2019-2020 school buses because seats may detach from the floor in a crash, increasing injury risk.
Sciegen Pharmaceuticals is recalling Irbesartan Tablets, 150 mg, because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).
Boston Scientific is recalling 12,900 SQ-RX Pulse Generators used in S-ICD systems due to latent internal battery malfunctions that cause accelerated depletion.
Honda is recalling 2019 Ridgeline and Pilot vehicles because a trim panel clip may interfere with right-side curtain air bag deployment in a crash.
Harvest Food Group is recalling Path of Life All Natural Southwest Quinoa due to potential contamination with Listeria monocytogenes or Salmonella.
Tosoh Bioscience is recalling seven AIA-2000 analyzers because a liquid suction pump defect may cause incomplete washing, leading to inaccurate test results.
Cadence Gourmet LLC is recalling Roasted Corn Salsa manufactured for Corner Bakery Café due to potential Salmonella and/or Listeria monocytogenes contamination.