State

Georgia product recalls

73,376 recalls have nationwide distribution and so reach Georgia. 9,621 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total: 9,621
Critical: 1,474
Severe: 2,561
Most recent: 2026-10-07

Of the 9,621 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 2,561 (27%) are Severe.

Which agencies issued them

These figures cover only the 9,621 recalls whose distribution notice names Georgia specifically. The 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18601–18625 of 82997

HighFDA (Drugs)·D-0459-2023·2023-03-22
Alprazolam Tablets Recalled Due to Potential Cross-Contamination Risk
Breckenridge Pharmaceutical is recalling multiple lots of Alprazolam 0.5mg tablets nationwide due to manufacturing process deviations that created a potential cross-contamination risk.
Product
Alprazolam Tablets, USP, 0.5mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0705-01), b) 500-count bottle (NDC 51991-0705-05) and c) 1,000-count bottle (NDC 51991-0705-10), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0581-2023·2023-03-22
Coffee pods with undeclared peanut residue being recalled
Two Rivers Coffee is recalling Brooklyn Bean Peanut Butter Cup Hot Cocoa pods because they may contain undeclared peanut residue. Consumers with peanut allergies should not use affected pods.
Product
Brooklyn Bean Peanut Butter Cup Hot Cocoa packaged in single serve pods. Pods are packaged in the following Brooklyn Beans Variety Pack boxes: Brooklyn Beans Hot Chocolate Variety Pack Pods, 12 Count UPC:810683021977 Brooklyn Beans Brooklyn Beans Peanut Butter Chocolate Hot…
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0460-2023·2023-03-22
Alprazolam Tablets Recalled for Potential Cross-Contamination from Manufacturing Deviations
Breckenridge Pharmaceutical is recalling Alprazolam 1 mg tablets distributed nationwide due to manufacturing practice deviations that pose a potential cross-contamination risk.
Product
Alprazolam Tablets, USP, 1 mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0706-01), b) 500-count bottle (NDC 51991-0706-05) and c) 1,000-count bottle (NDC 51991-0706-10), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0589-2023·2023-03-22
Cafe' Intermezzo Carrot Torte Recalled for Undeclared Food Colorants
Epic Baking is recalling Cafe' Intermezzo Carrot Torte because the product contains undeclared food colorants Yellow 5 and Red 40. The product was distributed in Georgia and Tennessee.
Product
Cafe' Intermezzo Carrot Torte 5.5 lbs Ingredients: Yellow Cake, Water, Carrots, Dark Brown Sugar, Vegetable Oil, Pecans, Walnuts, Cinnamon, Nutmeg, Allspice, Salt. Contains: Milk, eggs, tree nuts, wheat and soy, May contain peanuts.
Category
Food
Distribution
2 states
HighFDA (Food)·F-0608-2023·2023-03-22
Sunflower Lecithin Liquid Products Recalled for Undeclared Peanut Allergen
Navada Imports is recalling sunflower lecithin liquid in bulk totes due to undeclared peanut allergen. The affected products were distributed nationwide to food manufacturers.
Product
Sunflower Lecithin Liquid Packaged in 2,200 lb. (1,000 kg.) totes
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0617-2023·2023-03-22
Creamy Ranch Snack Mix Recalled for Metal Contamination
Catalina Snacks recalls Creamy Ranch flavored snack mix due to metal contamination. Consumers who have this product should not eat it.
Product
Creamy Ranch flavored ready-to-eat snack mix packaged in 6oz (UPC 850017468160) plastic stand up pouch.
Category
Food
Distribution
21 states
HighFDA (Drugs)·D-0458-2023·2023-03-22
Alprazolam Tablets Recalled for Potential Cross-Contamination Risk
Breckenridge Pharmaceuticals is recalling Alprazolam Tablets, USP 0.25mg distributed nationwide due to a potential cross-contamination risk from manufacturing deviations.
Product
Alprazolam Tablets, USP, 0.25mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0704-01), b) 500-count bottle and c) 1,000-count bottle, Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc.…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0584-2023·2023-03-22
Bakery Torte Recalled for Undeclared Espresso and Food Dyes
Epic Baking recalls Café Intermezzo Amaretto White Chocolate Tortes due to undeclared sub-ingredients: espresso, Yellow 5, and Yellow 6. These ingredients pose a risk to consumers with sensitivities.
Product
Cafe' Intermezzo Amaretto White Chocolate Torte 6.37 lbs Ingredient: White cake mix, vegetable oil, Amaretto syrup, Almond Extract, White chocolate flavor, Icing (Butter, Sugar, Amaretto syrup, Almond Extract, Vanilla Extract, white chocolate), Contains: Milk, eggs, wheat, soy…
Category
Food
Distribution
2 states
HighFDA (Food)·F-0597-2023·2023-03-22
Key Lime Cheesecake recalled for undeclared food dyes
Epic Baking is recalling Key Lime Cheesecake containing undeclared Yellow 5 and Blue 1 food dyes distributed to Georgia and Tennessee. Consumers with sensitivities may experience adverse reactions.
Product
Cafe' Intermezzo Key Lime Cheesecake 6.5 lbs Ingredients: Cream Cheese, Eggs, Sugar, Key Lime Mixture, Whipped Cream, Graham Cracker Crust (Graham Cracker Crumbs, Butter, Sugar, Vanilla Extract, Cinnamon), Key Lime Glaze (All-Purpose Flour, Nelly's Key Lime Juice, Vanilla…
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1242-2023·2023-03-22
BD Insulin Syringes Recalled for Nonsterile Condition and Infection Risk
Becton Dickinson is recalling 686,500 units of BD insulin syringes due to a nonsterile condition that may expose patients to pathogenic microorganisms and risk of infection.
Product
BD Insulin Syringes with the BD Micro-Fine IV Needle 0.5ml, 12.7mm, 28G Single Unit Scale-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 329461
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1247-2023·2023-03-22
TFN-Advanced Femoral Nails May Have Incorrect Length Markings
Synthes TFN-Advanced Femoral Nails labeled as 200mm may measure 170mm, and vice versa. Healthcare providers should verify actual dimensions before surgical use.
Product
TFN-Advanced Femoral Nail 12MM/125 DEG TI CANN TFNA 170MM - STERILE. Intended for temporary fixation and stabilization of proximal femur fractures. Part Number: 04.037.212S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0469-2023·2023-03-22
Eye allergy medication recalled for out-of-specification impurity
Teva Pharmaceuticals is recalling 715,632 bottles of Clear Eyes Once Daily eye drops due to an out-of-specification impurity found during stability testing.
Product
Clear Eyes, Once Daily, Eye Allergy Itch Relief, olopatadine hydrochloride ophthalmic solution, USP, 0.2%, Antihistamine, 2.5 mL (0.085 fl oz) bottle, Sterile, Distributed by Medtech Products Inc. Tarrytown, NY 10591, A Prestige Consumer Healthcare company, Made in Israel, UPC…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1243-2023·2023-03-22
BD Ultra-Fine Insulin Syringes Recalled Due to Nonsterile Condition
Becton Dickinson is recalling BD Ultra-Fine Insulin Syringes (Catalog Number 326719) due to a nonsterile condition that could expose patients to pathogenic microorganisms and local infection. Approximately 80,500 units distributed worldwide are affected.
Product
BD Ultra-Fine Insulin Syringe 1mL, 12.7mm, 29G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326719
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1245-2023·2023-03-22
Fusion Bioline Vascular Graft recalled due to manufacturing straightness defect
Maquet Cardiovascular is recalling one Fusion Bioline Vascular Graft from lot 25162546 that failed straightness testing. The graft could reduce blood flow or cause tension, potentially leading to bleeding and pseudo-aneurysm.
Product
Fusion Bioline Vascular Graft, Part number M00201503046B0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1258-2023·2023-03-22
Dimension Tacrolimus Diagnostic Cartridge Recalled for Measurement Imprecision
Siemens is recalling Dimension Tacrolimus diagnostic test cartridges (lots GA2286, GA3047, GA3171) due to confirmed measurement imprecision that could lead to incorrect drug dosing and potential organ failure or toxicity.
Product
Dimension Tacrolimus (TAC) Flex reagent cartridge-In vitro diagnostic test for the quantitative measurement of tacrolimus in human whole blood on the Dimension¿ clinical chemistry system SMN: 10700795 (DF207)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1257-2023·2023-03-22
Beckman Coulter Access Immunoassay Analyzers Recalled for Defective Nut Bands
Beckman Coulter is recalling approximately 4,100 laboratory immunoassay analyzers due to defective nut bands that may cause operational failures and erroneous patient test results.
Product
Access Immunoassay Systems (1) Access 2 Immunoassay Analyzer (81600N); (2) Access 2 Immunoassay Analyzer, Refurbished (386220); (3) Access 2 Immunoassay Analyzer, Refurbished (A65531) ; and (4) Access 2 Section, DxC 600i Packaged(A25640).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1237-2023·2023-03-22
BD Ultra-Fine Insulin Syringe Recall Due to Nonsterile Manufacturing
Becton Dickinson is recalling 45,000 units of BD Ultra-Fine Insulin Syringes (catalog 326679, lot 2164338) due to nonsterile manufacturing that could expose patients to pathogenic microorganisms and local infection. Distribution was worldwide.
Product
BD Ultra-Fine Insulin Syringe 0.5mL, 6mm, 31G - Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326679
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0621-2023·2023-03-22
Frozen Wonton Wrappers Recalled Due to Peanut Contamination in Sub-Ingredient
Bailey International Foods is recalling 4" x 4" and 3.5" x 3.5" frozen wonton wrappers due to peanut contamination in a sub-ingredient. The product was distributed to wholesalers in 19 states.
Product
Wonton wrappers, 4" x 4" and 3.5" x 3.5", packaged in 30lb. corrugated (cardboard) boxes. Product is sold frozen.
Category
Food
Distribution
19 states
HighFDA (Devices)·Z-1248-2023·2023-03-22
TFN Femoral Nails dimensions mislabeled, may measure 170mm or 200mm
Synthes recalled TFN-Advanced Femoral Nails because some units have incorrect dimensions: nails labeled 200mm may measure 170mm, while those labeled 170mm may measure 200mm. This dimensional mismatch could compromise surgical fixation.
Product
TFN-Advanced Femoral Nail 12MM/130 DEG TI CANN TFNA 170MM STERILE. Intended for temporary fixation and stabilization of proximal femur fractures Part Number: 04.037.242S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0618-2023·2023-03-22
Spicy Kick snack mix recalled due to potential metal contamination
Catalina Snacks is recalling Spicy Kick ready-to-eat snack mix pouches due to potential metal contamination. The product was distributed across multiple U.S. states and online sales.
Product
Spicy Kick flavored ready-to-eat snack mix packaged in 6oz (UPC 850017468153) plastic stand up pouch.
Category
Food
Distribution
21 states
HighFDA (Food)·F-0583-2023·2023-03-22
Celestial Seasonings Mandarin Orange Spice Tea Contains Undeclared Caffeine
Celestial Seasonings Mandarin Orange Spice herbal tea K-cups contain undeclared caffeine from black tea. The recall affects 1,844 units distributed nationwide.
Product
Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box
Category
Food
Distribution
42 states
HighFDA (Devices)·Z-1249-2023·2023-03-22
Plato 17 Microcatheter Recalled Due to Loose Particle Risk
Scientia Vascular is recalling Plato 17 Microcatheters due to manufacturing defects that may introduce loose particles into the catheter lumen, potentially causing blood vessel blockage or inflammatory reactions.
Product
Plato 17 Microcatheter: Straight Tip, PL17-160-000 ; 45 degree Tip, PL17-160-045; 90 degree Tip, PL17-160-090
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1255-2023·2023-03-22
Medical Device Apheresis Kit Recalled Due to Stress Leak Risk
Fenwal Inc is recalling 6,564 units in certain lots of Amicus apheresis kits because centrifuge packs may develop a stress leak. No illnesses or injuries have been reported.
Product
Amicus Exchange Kit Therapeutics. Component of Amicus Separator multiprocedural apheresis platform
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1250-2023·2023-03-22
Arial mobile application recalled for Android loading failures
Securitas Healthcare is recalling the Arial mobile application for Android devices because the app does not load or function properly. Users should stop using the app immediately.
Product
Arial mobile application, model #54630 and #54640 for Android devices downloaded from the Google Play Store as part of the Arial Emergency and Nurse Call system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0613-2023·2023-03-22
Chocolate Peanut Butter cereal recalled due to metal contamination
Catalina Snacks is recalling Chocolate Peanut Butter cereal (9oz pouches) due to metal contamination. The recall affects approximately 316,980 pouches distributed across multiple states and online retailers.
Product
Chocolate Peanut Butter flavored ready-to-eat cereal packaged in 9oz (UPC 850017468184) plastic stand up pouch.
Category
Food
Distribution
21 states