State
73,219 recalls have nationwide distribution and so reach Georgia. 9,620 additional recalls listed Georgia specifically in their distribution scope.
Of the 9,620 recalls naming Georgia we have scored against our rubric, 1,474 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,177 (23%) are Severe.
Which agencies issued them
These figures cover only the 9,620 recalls whose distribution notice names Georgia specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Alcon is recalling Legion FMS Pak surgical instruments due to reports of patient injuries caused by plastic debris generated from over-tightening with the included plastic wrench.
Covidien LP recalls MAHURKAR dialysis catheters due to excessive silicone lubricant on the catheter tip, which can obstruct the center lumen. This may delay treatment and cause serious blood complications including embolism and thrombosis.
A dialysis catheter product is being recalled due to excessive lubricant coating in the center lumen, which may cause full or partial obstruction. The blockage could delay treatment and increase risk of blood clots and hemolysis.
Covidien LP is recalling 5,373 MAHURKAR dialysis catheters because excessive silicone lubricant can occlude the catheter lumen, potentially causing treatment delays or blood clotting complications.
Covidien LP recalled 15,209 MAHURKAR dialysis catheters due to excessive lubricant in the center lumen, which may cause catheter occlusion, reduce blood flow, or lead to hemolysis and blood clots.
Covidien is recalling MAHURKAR acute dialysis catheters for excessive silicone lubricant causing lumen obstruction that may delay treatment and lead to hemolysis, embolism, or thrombosis.
Covidien's Mahurkar acute dialysis catheters may have excessive silicone lubricant causing tip obstruction. This could delay treatment or cause serious complications including blood clots and embolism.
Covidien LP is recalling MAHURKAR dialysis catheters because excessive silicone lubricant coats the center lumen, potentially blocking blood flow or creating clots and other blood vessel complications.
Covidien is recalling MAHURKAR dialysis catheters due to excessive silicone-based lubricant coating the center lumen tip, which may cause partial or complete obstruction, delaying treatment or causing thrombosis.
Covidien's MAHURKAR dialysis catheter is recalled because excessive silicone lubricant can block the center lumen, preventing or reducing blood flow during dialysis. This Class I recall affects 271 units and carries risk of treatment delays, hemolysis, and blood clots.
FreeStyle Libre 2 Readers may display an 'Incompatible Sensor' error when attempting to activate a new sensor after incomplete 14-day wear, potentially preventing new sensor activation and causing delayed glucose monitoring.
Lidl US TRADING is recalling Alpenfest Style Sachertote frozen dessert because egg, milk, and wheat allergens are not declared on the label. Consumers with allergies to these ingredients should not consume the product.
Olympus HF Resection Electrodes are being recalled due to reports of loop wire breakage when contacting metal objects. Broken fragments can fall inside the patient and require retrieval.
Hello wild strawberry fluoride toothpaste cartons contain tubes incorrectly labeled as hello fresh watermelon fluoride free toothpaste. 182,046 units affected nationwide.
Bentley is recalling 2017-2023 Bentayga vehicles because fuel supply module wiring can overheat, melt a flange, and cause a fuel leak that increases fire risk.
Olympus is recalling UroPass Ureteral Access Sheaths because dilator tips may break during surgical procedures or while in the package. The recall affects 9,520 units manufactured in 2018 and 2019.
Conformis hip screws measuring 30mm have been mislabeled as 25mm, creating risk of incorrect surgical implantation. The recall affects 25 units distributed across nine states.
Alcon Research recalls the Centurion FMS Pak following reports of patient injury during procedures. Plastic debris can result from over-tightening with the included plastic wrench.
Volkswagen is recalling 2024 Atlas and Atlas Cross Sport vehicles because engine bearings may fail, causing engine stalls and increasing the risk of crashes and fires.
Medtronic is recalling 44 units of the Duet External Drainage and Monitoring system because the product labels contain an incorrect expiration date. The affected lot (226632942) was distributed nationwide.
Alembic Pharmaceuticals is recalling 82,400 bottles of Tobramycin Ophthalmic Solution nationwide because the product failed to meet impurities and degradation specifications.
PLUVICTO (lutetium Lu 177 vipivotide tetraxetan) injection vials were labeled with incorrect lot numbers and expiration dates. The manufacturer is recalling affected lots distributed nationwide.
Harley-Davidson is recalling certain 2018–2023 Softail motorcycles where a fastener securing the rear shock absorber may break, causing tire damage and loss of tire pressure. This can lead to loss of vehicle control and increased crash risk.
Outfitter is recalling 2021-2022 truck campers because aluminum burner tubes may fracture, causing a gas leak that could lead to fire.
ATC is recalling 2022-2023 PL700 trailers because wire connections in the transfer switch may loosen, creating a fire risk from electrical overheat.