State

Georgia product recalls

73,817 recalls have nationwide distribution and so reach Georgia. 9,635 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total: 9,635
Critical: 1,471
Severe: 2,567
Most recent: 2026-11-04

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.

45801–45825 of 83452

SevereFDA (Drugs)·D-0208-2018·2018-01-17
Teva Recalls Moexipril Hydrochloride Tablets Due to Impurity Test Failure
Teva Pharmaceuticals is recalling specific bottles of Moexipril Hydrochloride and Hydrochlorothiazide tablets because routine stability testing found high levels of a degradation impurity.
Product
Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP, 7.5 mg/12.5 mg, 100-count bottle, Rx only, Distributed By: TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC 0093-5213-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0640-2018·2018-01-17
Jack Brown Produce Recalls Apples Due to Listeria Risk
Jack Brown Produce is voluntarily recalling multiple varieties of apples because they may be contaminated with Listeria monocytogenes.
Product
Golden Del., Gala, Fuji, Honey Crisp; Metric Tray sizes, 50ct, 55ct, 60ct, 78ct, 113ct, 2# Poly bags, 3# Poly bags and 5# Mesh bags; Trays-113ct (5trays per case), 55, 60, 78ct (2trays per RPC case) 2# & 3# - 12 bags per case, 5# - 8 bags per case
Category
Food
Distribution
5 states
SevereFDA (Food)·F-0637-2018·2018-01-17
Jack Brown Produce Recalls Gala Apples Due to Listeria Risk
Jack Brown Produce is voluntarily recalling specific lots of Gala apples due to potential Listeria monocytogenes contamination.
Product
Gala, whole fresh apples; Metric Tray sizes, 50ct, 55ct, 60ct, 78ct, 113ct, 2# Poly bags, 3# Poly bags and 5# Mesh bags; Trays-113ct (5trays per case), 55, 60, 78ct (2trays per RPC case) 2# & 3# - 12 bags per case, 5# - 8 bags per case
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-0322-2018·2018-01-17
CareFusion Recalls Alaris Syringe Pumps Due to Plunger Gripper Failure
CareFusion is recalling Alaris Syringe Pump Model 8110 units because the syringe plunger grippers may fail to close automatically, potentially affecting medication delivery.
Product
Alaris Syringe Pump, Model 8110. The firm name on the label is CareFusion. The Alaris Syringe Pump module and Alaris PCA module are infusion pump modules for the Alaris System. The syringe pump and PCA pump delivers medication or fluids in a manner similar to current syringe…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0324-2018·2018-01-17
Cordis S.M.A.R.T. Flex Biliary Stent System Recalled for Cracked Luer Hubs
Cordis Corporation is recalling 511 units of the S.M.A.R.T. Flex Biliary Stent System due to a potential for cracked luer hubs.
Product
Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated for use in the palliation of malignant strictures in the biliary tree.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0562-2018·2018-01-17
Harrisburg Dairies Recalls Egg Nog for Undeclared Egg Yolk Ingredient
Harrisburg Dairies is recalling 365 brand and Harrisburg Dairies brand Egg Nog because dried egg yolks were not listed in the ingredient statement.
Product
365 brand Egg Nog, Grade A; 1 qt. and 1/2 GAL; and Harrisburg Dairies brand Egg Nog, Grade A; 1/2 GAL, 1 Quart, 16 FL. OZ.
Category
Food
Distribution
14 states
HighFDA (Devices)·Z-0258-2018·2018-01-17
Orthoscan Mobile Mini C-arm System Recalled for Software Defect
Orthoscan is recalling Mobile Mini C-arm systems because a software defect allows users to activate Digital Zoom during live imaging, exposing a larger x-ray field than is visible to the user.
Product
Mobile Mini C-arm system Part # 1000-0001. Intended to provide the physician with general fluoroscopic visualization of the patient, including, but not limited to, surgical orthopedic procedures and critical and emergency care procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0259-2018·2018-01-17
Orthoscan Mobile Mini C-arm System Recalled for Software Defect
Orthoscan is recalling 2,012 Mobile Mini C-arm systems because a software defect allows users to activate Digital Zoom during live imaging, exposing a larger x-ray field than is visible to the user.
Product
Mobile Mini C-arm system Part # 1000-0004. Intended to provide the physician with general fluoroscopic visualization of the patient, including, but not limited to, surgical orthopedic procedures and critical and emergency care procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0560-2018·2018-01-17
Ingles Markets Recalls Frozen Biscuits for Listeria Contamination
Ingles Markets is recalling frozen Southern Style Biscuits after testing revealed Listeria monocytogenes contamination. The product was distributed in Georgia, North Carolina, South Carolina, and Tennessee.
Product
Frozen Southern Style Biscuits; 25 oz. bags (12 count)
Category
Food
Distribution
4 states
HighFDA (Food)·F-0561-2018·2018-01-17
Ingles Markets Recalls Frozen Buttermilk Biscuits Due to Listeria
Ingles Markets is recalling specific bags of frozen buttermilk biscuits because testing found Listeria monocytogenes. Consumers in Georgia, North Carolina, South Carolina, and Tennessee should not eat the product.
Product
Frozen Buttermilk Biscuits 25 oz. bag (12 count) and 44 oz. bag (20 count)
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-0321-2018·2018-01-17
Ambu Universal Flex2 Breathing Circuits Recalled for Leak Test Failures
King Systems Corp. dba Ambu, Inc. is recalling 871,116 Universal Flex2 Breathing Circuits due to potential leak test failures.
Product
UNIVERSAL FLEX2 BREATHING CIRCUIT, Item Numbers: D460-6133Z, D390-6121Z, D390-6121Z, D495-61Z, DF4116-6121Z, D466-61Z, DFP170-6121, DF3115-6121Z, DF375-6121Z, DF3115-6121Z, DF3115-6121Z, D360-8031Z, D465-61Z, JD365-6033Z, DF370-6121Z, DF3110-61Z, DF375-17621Z, DF375-6121Z…
Category
Medical Device
Distribution
43 states
HighFDA (Devices)·Z-0261-2018·2018-01-17
OrthoScan Recalls Mobile Mini C-arm Systems Due to Software Defect
OrthoScan is recalling 2,012 Mobile Mini C-arm systems because a software defect allows users to activate Digital Zoom during live imaging, exposing a larger x-ray field than visible.
Product
Mobile Mini C-arm system Part # 1000-0004-FD. Intended to provide the physician with general fluoroscopic visualization of the patient, including, but not limited to, surgical orthopedic procedures and critical and emergency care procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0318-2018·2018-01-17
Repro-Med HIgH-Flo Subcutaneous Safety Needle Sets Recalled for Packaging Defects
Repro-Med Systems is recalling HIgH-Flo Subcutaneous Safety Needle Sets because gaps were found in the sterile barrier packaging during post-sterilization inspection.
Product
HIgH-Flo Subcutaneous Safety Needle Sets, 2-Needle Set/ 24 Gauge 9mm Needles, REF/Part Numbers RMS22606, RMS22609, RMS22612, RMS12606, RMS22409, RMS32609, RMS32609, RMS12409, RMS12609, RMS62612, RMS62606, RMS12406, RMS22412, RMS12412, RMS42606, RMS62609, RMS52612, RMS42612…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0323-2018·2018-01-17
CareFusion Alaris PCA Pump Recall Due to Syringe Plunger Gripper Failure
CareFusion is recalling Alaris PCA Pumps because the syringe plunger grippers may fail to close automatically, potentially affecting medication delivery.
Product
Alaris PCA Pump, Model 8120. The firm name on the label is CareFusion. The Alaris Syringe Pump module and Alaris PCA module are infusion pump modules for the Alaris System. The syringe pump and PCA pump delivers medication or fluids in a manner similar to current syringe…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0317-2018·2018-01-17
Repro-Med Systems Recalls Freedom60 Precision Flow Rate Tubing Sets
Repro-Med Systems is recalling Freedom60 Precision Flow Rate Tubing Sets and related needle sets because gaps were found in the sterile barrier packaging during inspection.
Product
Freedom60 Precision Flow Rate Tubing Sets, REF/Part Numbers F900, F2400, F60, F10, F275, F600, F45, F1200 F180.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0260-2018·2018-01-17
OrthoScan Recalls Mobile Mini C-arm Systems Due to Software Defect
OrthoScan is recalling 2,012 Mobile Mini C-arm systems because a software defect allows users to activate Digital Zoom during live imaging, exposing a larger x-ray field than visible.
Product
Mobile Mini C-arm system Part # 1000-0005. Intended to provide the physician with general fluoroscopic visualization of the patient, including, but not limited to, surgical orthopedic procedures and critical and emergency care procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0190-2018·2018-01-17
KRS Global Biotechnology Recalls QUADMIX #17 Due to Expired Ingredients
KRS Global Biotechnology is recalling 122 vials of QUADMIX #17 because the product's beyond-use date exceeds the expiration date of at least one ingredient.
Product
QUADMIX #17, 5 mL Vial, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0182-2018·2018-01-17
KRS Global Biotechnology Recalls Iodochlorhydroxyquin Otic Powder Due to Labeling Error
KRS Global Biotechnology is recalling 40 jars of Iodochlorhydroxyquin Otic Powder because the Beyond Use Date exceeds the expiration of at least one ingredient.
Product
Iodochlorhydroxyquin 3%/ Boric Acid 10%/ Amphotericin 5% Otic Powder packaged in jars, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0171-2018·2018-01-17
KRS Global Biotechnology Recalls Chloramphenicol Otic Powder Due to Labeling Errors
KRS Global Biotechnology is recalling 100 jars of Chloramphenicol Otic Powder because the Beyond Use Date exceeds the expiration date of at least one ingredient.
Product
Chloramphenicol 500 mg Sulfamethoxazole 500 mg Amphotericin 50 mg Otic Powder packaged in jars, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0174-2018·2018-01-17
KRS Global Biotechnology Recalls Human Chorionic Gonadotropin Vials for Labeling Errors
KRS Global Biotechnology is recalling 1,203 vials of Human Chorionic Gonadotropin due to incorrect or missing lot and expiration dates.
Product
Human Chorionic Gonadotropin 2,500 Units, Vial-Lyophilized, For SC Use, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0166-2018·2018-01-17
KRS Global Biotechnology Recalls Topical Cream Due to Expired Ingredients
KRS Global Biotechnology is recalling 1,380 jars of Benzocaine, Lidocaine, and Tetracaine Topical Cream because the product's beyond-use date exceeds the expiration dates of its ingredients.
Product
Benzocaine 20%, Lidocaine 8%, Tetracaine 4% Topical Cream packaged in jars, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0178-2018·2018-01-17
KRS Global Biotechnology Recalls Human Chorionic Gonadotropin Vials for Labeling Errors
KRS Global Biotechnology is recalling 2,274 vials of Human Chorionic Gonadotropin 20,000 iu due to incorrect or missing lot and expiration dates.
Product
Human Chorionic Gonadotropin 20,000 iu/Vial, Lyophilized - For SC Use, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0200-2018·2018-01-17
KRS Global Biotechnology Recalls T-105 Vials Due to Expired Ingredient Dates
KRS Global Biotechnology is recalling 173 vials of T-105 because the Beyond Use Date exceeds the expiration of at least one ingredient.
Product
T-105 (Prostaglandin E1, 10 mcg/ Papaverine 30 mg/ Phentolamine 1 mg/mL), For Intracavernouse Use, 5 mL Vial, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0202-2018·2018-01-17
KRS Global Biotechnology Recalls Ophthalmic Solution Due to Labeling Errors
KRS Global Biotechnology is recalling 81 droptainers of a multi-dose ophthalmic solution because the Beyond Use Date exceeds the expiration date of at least one ingredient.
Product
Cyclopentolate HCl/ Phenylephrine HCl/ Tropicamide/ Ketorolac 1%/ 10%/ 1%/ 0.5% Ophthalmic Soln, 5 mL Multi Dose Droptainer, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0187-2018·2018-01-17
KRS Global Biotechnology Recalls Prednisolone Tablets Due to Labeling Errors
KRS Global Biotechnology is recalling 3,000 Prednisolone 10 mg tablets because the expiration date exceeds the stability of an ingredient.
Product
PrednisoLONE 10 mg Tablet, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide