State
73,737 recalls have nationwide distribution and so reach Georgia. 9,632 additional recalls listed Georgia specifically in their distribution scope.
Of the 9,632 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 2,565 (27%) are Severe.
Which agencies issued them
These figures cover only the 9,632 recalls whose distribution notice names Georgia specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Daimler Vans is recalling 2018-2019 Mercedes-Benz and Freightliner Sprinter vehicles because the spare tire label may list the maximum speed in kilometers per hour instead of miles per hour.
H J Harkins Company Inc is recalling Acetaminophen 500 mg tablets because a foreign Women's Prenatal tablet was found in the product.
Cardinal Health is recalling Monoject 3mL syringes with safety needles because they were shipped as non-sterile despite labeling. The firm is not aware of any patient harm reports.
Earth Sonnets is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.
Stonewall Kitchen is recalling Ghost Pepper Salsa because it contains undeclared milk and soy allergens. Consumers should check their pantry for the specific product.
Lamborghini is recalling 26 2020 Aventador SVJ vehicles because the interior door handle mechanism may fail, preventing the door from opening from inside.
SeeNext Venture is recalling NumbSkin pain relief cream because the packaging is not child-resistant, posing a risk of poisoning to young children.
Daimler Vans USA is recalling 2018-2019 Sprinter vans because the spare tire may lack a maximum speed label, increasing the risk of tire failure.
Medicrea International is recalling 3,529 Iliac Screws because an internal component was assembled incorrectly, which may cause the tulip head to disengage from the shank.
Medtronic is recalling six Simulus 850 Semi Rigid Ring/Band Accessory Kits because demonstration units may have contacted porcine tissue.
Earthroma is recalling Wintergreen Essential Oil bottles because the packaging is not child-resistant, posing a poisoning risk to young children.
EHOB, Inc. is recalling specific lots of Econocare Plus Waffle Overlays due to potential contamination with human blood. No instances of contamination have been confirmed in distributed products.
Novartis is recalling 100 mg Sandimmune and Neoral blister packages because they fail child-resistant packaging requirements, posing a poisoning risk to children.
Medicrea International is recalling 3,529 pedicle screws because an internal component was assembled incorrectly, which may cause the tulip head to disengage from the screw shank.
Belle Chemical is recalling sodium and potassium hydroxide products because they lack required child-resistant packaging and proper hazard labeling.
ARJOHUNTLEIGH is recalling 669 Concerto and Basic Shower Trolleys because a mechanical failure in the safety catch could cause the side support to open, posing a risk of patient falls and injuries.
BMW is recalling 2018-2020 X3 and 2019-2020 X4 vehicles because the instrument panel casing may not be tightened properly, posing an injury risk during air bag deployment.
Cardinal Health is recalling Monoject Hypodermic Safety Needles because they were shipped as non-sterile despite labeling indicating sterility, posing an infection risk.
Cardinal Health 200, LLC is recalling Monoject Bluntfill syringes that were shipped as non-sterile but labeled as sterile. The firm is not aware of any patient harm.
Medtronic CoreValve LLC is recalling six Simulus 750 Flexible Ring/Band Accessory Kits because demonstration units may have contacted non-human tissue.
The Boyer Corporation is recalling six brands of sodium and potassium hydroxide products because the packaging is not child-resistant, posing a risk of chemical burns.
Lupin Pharmaceuticals is recalling specific lots of oral contraceptive tablets due to failed content uniformity tests.
Verathon, Inc. is recalling 239 GlideScope Video Laryngoscope Operations & Maintenance Manuals due to a typographical error regarding disinfection instructions.
Response Biomedical Corp. is recalling RAMP Cardiac Controls because CK-MB levels decreased by up to 57% within 11 months, potentially affecting quality control results.
Braemar Manufacturing is recalling DL950 Holter Monitors because a software issue prevents new patient studies from starting.