Product Recalls in Georgia

Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,585 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,585 in last 12 months

Showing 761780 of 53,623 recalls

DrugNovember 6, 2025· Fresenius Kabi USA, LLC

Recalled Item: Famotidine Injection Recalled by Fresenius Kabi USA, LLC Due to Microbial...

The Issue: Microbial Contamination of Sterile Products; out of limit results obtained...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 6, 2025· VENTURA FOODS LLC

Recalled Item: Italian Salad Dressing Recalled by VENTURA FOODS LLC Due to Foreign Object...

The Issue: foreign objects (black plastic planting material) in granulated onion

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 6, 2025· VENTURA FOODS LLC

Recalled Item: Publix Deli Carolina-Style Mustard BBQ Sauce Recalled by VENTURA FOODS LLC...

The Issue: foreign objects (black plastic planting material) in granulated onion

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 6, 2025· C.R. Bard Inc

Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm Recalled by C.R. Bard...

The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· CareFusion 303, Inc.

Recalled Item: BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The Recalled...

The Issue: Due to a number of modules flashed with a date and time associated with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· C.R. Bard Inc

Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm Recalled by C.R. Bard...

The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· Bard Peripheral Vascular Inc

Recalled Item: Safe-T-Centesis 6 Fr Catheter Drainage Tray Recalled by Bard Peripheral...

The Issue: Acute drainage catheters, indicated for use in removing fluid during acute...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Accriva Diagnostics, Inc.

Recalled Item: Hemochron Activated Clotting Time Low-Range Test Cuvette Recalled by Accriva...

The Issue: Test cuvettes, used with an assay for monitoring heparin anticoagulation,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Diasol, Inc

Recalled Item: Brand Name: Diasol Product Name: 100125-10-DEX100 Recalled by Diasol, Inc...

The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Cepheid

Recalled Item: Xpert MTB/RIF. Model Number: GXMTB/RIF-US-10. Recalled by Cepheid Due to...

The Issue: Product testing did not meet expected stability criteria.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Diasol, Inc

Recalled Item: Brand Name: Diasol Product Name: 100230-10-DEX100 Recalled by Diasol, Inc...

The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Diasol, Inc

Recalled Item: Brand Name: Diasol Product Name: 100325-10-DEX100 Recalled by Diasol, Inc...

The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugNovember 5, 2025· Lupin Pharmaceuticals Inc.

Recalled Item: Sertraline Hydrochloride Tablets USP Recalled by Lupin Pharmaceuticals Inc....

The Issue: Defective container - seal not adhering to bottles

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 5, 2025· Diasol, Inc

Recalled Item: Brand Name: Diasol Product Name: 100425-10-DEX100 Recalled by Diasol, Inc...

The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Diasol, Inc

Recalled Item: Brand Name: Diasol Product Name: 100225-10-DEX100 Recalled by Diasol, Inc...

The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Diasol, Inc

Recalled Item: Brand Name: Diasol Product Name: 100220-10-DEX100 Recalled by Diasol, Inc...

The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2025· Datascope Corp.

Recalled Item: Cardiosave Hybrid. Intra-Aortic Balloon Pump system. Recalled by Datascope...

The Issue: The IFU addendum revises the Preventative Maintenance schedule to align with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2025· Datascope Corp.

Recalled Item: Cardiosave Rescue. Intra-Aortic Balloon Pump system. Recalled by Datascope...

The Issue: The IFU addendum revises the Preventative Maintenance schedule to align with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodNovember 4, 2025· Tai Phat Wholesalers, LLC

Recalled Item: Sofit Recalled by Tai Phat Wholesalers, LLC Due to Undeclared Sulfites

The Issue: Undeclared sulfites

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Neurotransmitters Plus Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing