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.
Amerisource Health Services is recalling specific lots of Paroxetine tablets because they contain foreign tablets or capsules.
Shoreline Fruit is voluntarily recalling dark chocolate covered cherry products due to undeclared milk in the dark chocolate coating.
Medline Industries is recalling 1,428 Transfer/Gait Belts because the locking mechanism may fail to secure the strap, allowing it to slip through the buckle.
3M is recalling Bair Hugger temperature sensors because a programming error may cause the device to display a temperature lower than the patient's actual body temperature.
Zimmer Biomet is recalling 64 ROSA Surgical Device 2.5.8 units because a software defect may change tool orientation without user command.
Medline Industries is recalling 8,000 units of Sensicare Green Surgical Gloves because a possible open seal on the packaging could compromise sterility.
Halyard Health is recalling Turbo-Cleaning Closed Suction Systems because saline vials may leak, potentially exposing contents to infectious agents.
Ford is recalling 2016 Explorer and F-150 vehicles because loose seat bolts may cause cushions to detach in a crash, increasing injury risk.
Halyard Health is recalling specific lots of Closed Suction Systems because saline vials may leak, potentially exposing contents to infectious agents.
Toyota is recalling 2015-2018 4Runners with specific accessory grille overlays because a securing nut may fracture, causing the part to detach and create a road hazard.
Halyard Health is recalling NOVAPLUS Endotracheal WET PAK Closed Suction Systems because 15ml saline vials may leak, potentially exposing contents to infectious agents.
Toys R Us is recalling approximately 6,000 'totally me!' clay craft kits sold at Babies R Us and Toys R Us stores because the clay may contain mold, posing a risk of respiratory or other infections.
Halyard Health is recalling specific lots of Closed Suction Systems because 15ml saline vials may leak, potentially exposing contents to infectious agents.
Halyard Health is recalling specific lots of saline vials used in closed suction systems because they may leak, potentially exposing the contents to infectious agents.
Halyard Health is recalling Turbo-Cleaning Closed Suction Systems because 15ml saline vials may leak, potentially exposing contents to infectious agents.
Medline Industries is recalling 190 units of pediatric elbow closed suction catheters because they were distributed before being sterilized.
Halyard Health is recalling specific lots of saline vials used in closed suction systems because they may leak, potentially exposing contents to infectious agents.
Shoreline Fruit is voluntarily recalling dark chocolate covered cherries because the supplier recalled dark chocolate containing undeclared milk.
Halyard Health is recalling specific lots of Closed Suction Systems because the saline vials may leak, potentially exposing contents to infectious agents.
Astor Chocolate Corporation is recalling Dark Chocolate Covered Cranberries due to an undeclared milk allergen. The product was distributed across multiple US states and Canada.
Libbey Glass is recalling approximately 229,000 Bourbon Taster Glasses because they can break during normal use, posing a laceration hazard.
Medline Industries is recalling 1,428 plastic transfer belts because the locking mechanism may fail, allowing the strap to slip through the buckle.
Medline Industries is recalling 120 units of sterile suction catheters that were distributed before being sterilized.
Zimmer Biomet is recalling 29 ROSA Surgical Devices due to a software issue affecting cooperative endoscopy mode.
Leading Pharma, LLC is recalling Lorazepam tablets labeled as 0.5 mg but containing 1 mg. The recall addresses a labeling error affecting 2,952 bottles nationwide.