State

Georgia product recalls

72,971 recalls have nationwide distribution and so reach Georgia. 9,588 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total: 9,588
Critical: 1,464
Severe: 2,164
Most recent: 2026-09-09

Of the 9,588 recalls naming Georgia we have scored against our rubric, 1,464 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,164 (23%) are Severe.

Which agencies issued them

These figures cover only the 9,588 recalls whose distribution notice names Georgia specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5876–5900 of 82559

CriticalFDA (Devices)·Z-2328-2025·2025-08-27
Hamilton C6 ventilators recalled over circuit board defect interrupting ventilation
Hamilton C6 ventilators are recalled over a mechanical defect on a printed circuit board that may cause the device to fail at startup or interrupt ventilation during use. 1,040 systems are affected.
Product
Hamilton C6 REF 160021 (ESM Board PN 10144626 UDI-DI code: 76300028PN160021ZW Hamilton C6 is a ventilator intended to provide positive pressure ventilatory support to adults and pediatrics and optionally infants and neonates.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0514-2025·2025-08-27
Cinnamon pecan fritters recalled because egg is missing from allergen labeling
Hillside Orchard Farms Cinnamon Pecan Fritters, 7 oz, are recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Product
Cinnamon Pecan Fritters Net Weight 7 oz (198g) CONTIANS: Wheat, Soybeans, Milk & Pecans Made By: Hillside Orchard Farms 105 Mitcham Circle Tiger, GA 30576
Category
Food
Distribution
5 states
CriticalFDA (Food)·H-0519-2025·2025-08-27
Strawberry fritters recalled over undeclared egg omitted from the label
Hillside Orchard Farms Strawberry Fritters, 7 oz, are recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Product
Strawberry Fritter Net Wt 7oz (198g) CONTAINS: Wheat, Soybeans, Milk. Made By: Hillside Orchard Farms 105 Mitcham Circle Tiger, GA 30576
Category
Food
Distribution
5 states
CriticalFDA (Devices)·Z-2326-2025·2025-08-27
ENDOTAK RELIANCE leads with 4-SITE connector recalled over coil calcification
ENDOTAK RELIANCE G/SG defibrillation leads with the 4-SITE connector are recalled because affected models may show gradually rising LVSI measurements linked to calcification of the defibrillation coils.
Product
ENDOTAK RELIANCE G/SG with 4-SITE Connector, transvenous defibrillation lead, Permanent Defibrillator Electrodes; Model Nos. 0282, 0283, 0285, 0286, 0292, 0293, 0295, 0296
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0517-2025·2025-08-27
Peach fritters recalled over undeclared egg missing from the ingredient label
Hillside Orchard Farms Peach Fritters, 7 oz, are recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Product
Peach Fritter Net Weight 7 oz (198g) CONTAINS: Wheat, Soybeans, & Milk. Made By: Hillside Orchard Farms 105 Mitcham Circle Tiger, GA 30576
Category
Food
Distribution
5 states
CriticalFDA (Devices)·Z-2325-2025·2025-08-27
ENDOTAK RELIANCE defibrillation leads recalled over coil calcification and rising LVSI
ENDOTAK RELIANCE G/SG transvenous defibrillation leads are recalled because affected models may show gradually rising LVSI measurements linked to calcification of the defibrillation coils.
Product
ENDOTAK RELIANCE G/SG, transvenous defibrillation lead, implantable cardioverter defibrillator (non-CRT); Model Nos. 0160, 0161, 0162, 0163, 0164, 0165, 0166, 0167, 0170, 0171, o182, 0173, 0174, 0175, 0176, 0177, 0180, 0182, 0183, 0184, 0185, 0186, 0187
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2327-2025·2025-08-27
RELIANCE 4-FRONT defibrillation leads recalled over rising LVSI measurements and coil calcification
RELIANCE 4-FRONT defibrillation leads are recalled because affected models may show gradually rising LVSI measurements linked to calcification of the defibrillation coils, which may lead to early lead replacement.
Product
RELIANCE 4-FRONT, endocardial cardioversion/defibrillation and pace/sense lead, Permanent Defibrillator Electrodes; Model Nos. 0654, 0655, 0657, 0658, 0682, 0683, 0685, 0686, 0692, 0693, 0695, 0696
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0518-2025·2025-08-27
Strawberry bread recalled for undeclared egg not listed among allergens
Hillside Orchard Farms Strawberry Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Product
Strawberry Bread Net Wt. 23 oz (652 G) CONTAINS: MILK, SOY, & WHEAT HILLSIDE ORCHARD FARMS 105 Mitcham Circle, Tiger GA 30576
Category
Food
Distribution
5 states
CriticalFDA (Food)·H-0507-2025·2025-08-27
Apple fritters recalled because egg is not declared on the label
Hillside Orchard Farms Apple Fritters, 7 oz, are recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Product
Apple Fritter Contains: Wheat, Soy and Milk Made By: Hillside Orchard Farms 105 Mitcham Circle Tiger, GA 30576
Category
Food
Distribution
5 states
CriticalFDA (Food)·H-0513-2025·2025-08-27
Cinnamon pecan bread recalled because egg is undeclared on the package
Hillside Orchard Farms Cinnamon Pecan Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Product
Cinnamon Pecan Bread Net Wt. 23 oz (652 G) CONTAINS: MILK, SOY & WHEAT. HILLSIDE ORCHARD FARMS 105 Mitcham Circle, Tiger GA 30576
Category
Food
Distribution
5 states
CriticalFDA (Food)·H-0509-2025·2025-08-27
Fresh blackberry bread recalled because egg is not declared on label
Hillside Orchard Farms Fresh Blackberry Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Product
Fresh Blackberry Bread Net Wt. 23 oz (652 G) CONTAINS: MILK, SOY, & WHEAT HILLSIDE ORCHARD FARMS 105 Mitcham Circle, Tiger GA 30576
Category
Food
Distribution
5 states
CriticalFDA (Food)·H-0510-2025·2025-08-27
Blueberry bread recalled over egg that is not declared on label
Hillside Orchard Farms Blueberry Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Product
Blueberry Bread Net Wt. 23 oz (652 G) CONTAINS: MILK, SOY, & WHEAT HILLSIDE ORCHARD FARMS 105 Mitcham Circle, Tiger GA 30576
Category
Food
Distribution
5 states
CriticalFDA (Food)·H-0512-2025·2025-08-27
Cheese bread recalled over undeclared egg absent from Contains statement
Hillside Orchard Farms Cheese Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Product
Cheese Bread Net Wt. 23 oz (652 G) CONTAINS: MILK, SOY & WHEAT. HILLSIDE ORCHARD FARMS 105 Mitcham Circle, Tiger GA 30576
Category
Food
Distribution
5 states
CriticalFDA (Food)·H-0508-2025·2025-08-27
Banana nut bread recalled for undeclared egg in the ingredient labeling
Hillside Orchard Farms Banana Nut Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Product
Banana Nut Bread Net. Wt 23 oz (653g) CONTAINS: MILK, SOY, WHEAT & PECANSHILLSIDE ORCHARD FARMS 105 Mitcham Circle, Tiger GA 30576
Category
Food
Distribution
5 states
CriticalFDA (Food)·H-0515-2025·2025-08-27
Jalapeno cheese bread recalled over undeclared egg in Hillside Orchard product
Hillside Orchard Farms Jalapeno Cheese Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Product
Jalapeno Cheese Bread Net Wt. 23 oz (652 G) CONTAINS: MILK, SOY & WHEAT. HILLSIDE ORCHARD FARMS 105 Mitcham Circle, Tiger GA 30576
Category
Food
Distribution
5 states
CriticalFDA (Food)·H-0511-2025·2025-08-27
Blueberry fritters recalled for undeclared egg absent from the product label
Hillside Orchard Farms Blueberry Fritters, 7 oz, are recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Product
Blueberry Fritter Net Wt 7 oz (198g) CONTAINS: MILK, SOY, WHEAT. Made By: Hillside Orchard Farms 105 Mitcham Circle Tiger, GA 30576
Category
Food
Distribution
5 states
SevereNHTSA·25V556000·2025-08-27
2026 BMW X5, X7 Plug-in Hybrid Windshield Seal Water Leak Recall
BMW is recalling certain 2026 X5, X5 Plug-in Hybrid, and X7 vehicles because the windshield may not be sealed properly, allowing water to enter electrical components and potentially causing headlight failure or fire.
Product
BMW — BMW X5 PLUG-IN HYBRID, X5, X7
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2338-2025·2025-08-27
Electrosurgical generators recalled over system error causing reboots during use
The ESG-410 Electrosurgical Generator is recalled because it may display an E0662 System Error followed by a single automatic reboot or a continuous reboot loop. 155 units are affected.
Product
Electrosurgical, Cutting and Coagulation and Accessories. Electrosurgical Generator ESG-410 Surgical Energy Platform (SEP). Model Number: WA91327U. The ESG-410 Electrosurgical Generator is an electrosurgical generator which utilizes monopolar and bipolar high frequency current
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2340-2025·2025-08-27
Deep brain stimulation burr hole kits recalled over retaining clip closing resistance
Burr Hole Cover Kits used with the Vercise Deep Brain Stimulation System are recalled because resistance closing the retaining clip may cause procedural delay or lead migration requiring further surgery. 24,583 units are affected.
Product
Burr Hole Cover Kit, REF: M365DB4600C0; Burr Hole Cover Spares Kit, REF: M365DB4605C0. Components of Vercise Deep Stimulation System used with the Surgical Implant Manual
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2336-2025·2025-08-27
Estrone diagnostic kits recalled over rare falsely high or low results
Estrone RIA kits, catalog number DSL8700, are recalled because certain lots may rarely give falsely high or falsely low patient results. 279 units are affected.
Product
Estrone RIA Catalog Number DSL8700 UDI Code: 15099590211615 Estrone RIA is an in vitro diagnostic manual medical device used by healthcare professionals for the quantitative measurement of estrone in human serum and plasma.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0591-2025·2025-08-27
Sodium bicarbonate injection vials recalled for lack of assurance of sterility
Hospira 8.4% Sodium Bicarbonate Injection USP, 50 mEq/50 mL, lot LH2671, is recalled nationwide for lack of assurance of sterility. 15,750 vials are affected.
Product
SODIUM BICARBONATE — SODIUM BICARBONATE (SODIUM BICARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0504-2025·2025-08-27
Zero sugar soda cans recalled because they contain full sugar product
7up Zero Sugar Tropical Soda in 12 fl oz cans is recalled because the cans are labeled Zero Sugar but contain full sugar product. 1,954 cases are affected.
Product
7up Zero Sugar Tropical Soda, 12 FL OZ (355 mL) aluminum cans, packaged in 12 pack cardboard cartons labeled as 7up Tropical Flavored Soda, UPC (on can): 078000037975, UPC (on carton): 078000037982
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-2331-2025·2025-08-27
Bayonet injection needles recalled after showing elevated cytotoxicity in testing
Bayonet Luer-Lock injection needles, models 50-353-23 and 50-345-23, are recalled because affected product showed elevated cytotoxicity values, which may present a risk of intolerance or allergic reaction.
Product
Injection needle, bayonet, Luer-Lock, 1. Model no. 50-353-23, working length 25 cm, total length 31cm, nonsterile; 2. Model no. 50-345-23, working length 24 cm, total length 31 cm, non-sterile
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0594-2025·2025-08-27
Major Pharmaceuticals carvedilol tablets recalled over nitrosamine impurity above FDA limit
Carvedilol Tablets USP, 12.5 mg, packaged by Major Pharmaceuticals, lot T05693, are recalled nationwide because N-Nitroso Carvedilol Impurity-1 exceeded the FDA-recommended 4.0 ppm limit. 26,628 cartons are affected.
Product
CARVEDILOL — CARVEDILOL (CARVEDILOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0505-2025·2025-08-27
Ojasvita Chocomalt 200 g pouches recalled for undeclared soy lecithin
Sri Sri Tattva Ojasvita Chocomalt, 7 oz / 200 g paper pouches, is recalled because it contains undeclared soy lecithin. 1,100 units are affected.
Product
Sri Sri Tattva, Ojasvita Chocomalt,7oz / 200g, Paper Pouch, 25 packages per case
Category
Food
Distribution
10 states