State
73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
TeDan Surgical Innovations is recalling 3COR Distraction Screws because the sterile pouch seal is defective, potentially compromising sterility.
Teleflex is voluntarily recalling 6,014 RUSCH LASERTUBE devices because the laser guard foil may partially separate or detach at the edges when exposed to moisture.
Somerset Therapeutics is recalling Brimonidine Tartrate Ophthalmic Solution 0.2% due to a slow leaching process from the product label that may impact the product over its shelf life.
Somerset Therapeutics is recalling 383,437 bottles of Brimonidine Tartrate Ophthalmic Solution 0.2% because a slow leaching process from the product label may impact the product over its shelf life.
Somerset Therapeutics is recalling Brimonidine Tartrate Ophthalmic Solution 0.2% due to a slow leaching process from the product label that may impact the product over its shelf life.
Daimler Coaches North America is recalling 2018-2020 Setra motorcoaches because the Electronic Stability Control system can be disabled at unsafe speeds, increasing crash risk.
Daimler Trucks North America is recalling 16,776 Freightliner Custom Chassis vehicles because a damaged Power Distribution Module may cause rear lights to fail, increasing crash risk.
Jayco is recalling specific 2016-2018 motorhomes because a mounting bracket for the leveling system may fail, allowing components to contact the ground and increasing crash risk.
Curt Manufacturing is recalling Rambler RV Towbars because the axial pivot pin may loosen or fail, potentially causing the hitch to separate and increasing crash risk.
Gulf Stream is recalling 2020-2021 Super-Lite 19RD travel trailers because the rear axle may contact the black water tank, causing spills and crash risks.
Mitsubishi is recalling 2014-2019 Outlander and 2018-2019 Outlander PHEV vehicles because the second-row center seat belt buckle may interfere with the right-side buckle, rendering it inoperable.
Forest River is recalling specific 2021 Riverstone trailers equipped with an optional generator prep package due to incorrect transfer switch wiring that may cause voltage back feed.
Altec is recalling 2017-2020 aerial devices due to a power take-off that may leak oil onto the exhaust heat shield, increasing fire risk.
RH is recalling Riveted Mesh Floor Lamps because the foot switch can overheat or catch fire. Consumers should stop using the lamps and contact RH for a refund.
Ananda Apothecary is recalling four essential oil products because their packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.
Miracle Botanicals is recalling Wintergreen and Birch Essential Oils because the packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.
Cooper Lighting is recalling about 39,000 All Field and Prism RGBA light fixtures because lenses can loosen and fall, posing an injury risk to people below.
DaVinci is recalling about 3,000 Bailey bassinets because the mattress support can disengage, posing fall and entrapment risks to infants.
Beyond Better Foods is recalling Enlightened Dairy-Free Chocolate Peanut Butter Frozen Dessert because it may contain undeclared milk.
Mount Franklin Foods is recalling 7-Select Yogurt Pretzels because they may contain undeclared peanuts. The product was distributed to 7-11 stores nationwide.
LivaNova is recalling eight SCP Pump Control Panels because premature wear of the angle encoder may make the rotary knob difficult or impossible to rotate during cardiopulmonary bypass.
Beaming White LLC is recalling Koala Hand Sanitizer because the ethanol content is below the label claim and undeclared isopropyl alcohol is present.
LivaNova is recalling 24 SCP Pump Control Panels because the rotary knob may fail to rotate due to premature wear, risking patient injury during surgery.
LivaNova USA Inc. is recalling 150 units of Vein Irrigation Cannulas with blunt tips because internal tests identified potential breaches in the sterile barrier.
Beaming White LLC is recalling Koala Hand Sanitizer because the ethanol level is below the label claim and it contains undeclared isopropyl alcohol.