Product Recalls in North Carolina

Product recalls affecting North Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to North Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,828 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
2,828 in last 12 months

Showing 18411860 of 54,363 recalls

DrugJuly 25, 2025· Alembic Pharmaceuticals Limited

Recalled Item: Doxepin Hydrochloride Capsules Recalled by Alembic Pharmaceuticals Limited...

The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 25, 2025· Home Health US, Incorporated

Recalled Item: One Step Sterile Lancet for Single Use (3 sizes): 06949517008861 Recalled by...

The Issue: Due to incorrect/lack of Unique Device Identifier (UDI) codes.

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

Class III — Low RiskOngoing
Medical DeviceJuly 25, 2025· Zap Surgical Systems

Recalled Item: ZAP-X Radiosurgery System Recalled by Zap Surgical Systems Due to If the...

The Issue: If the radiosurgery system triggers a proximity error message during a long...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2025· Merit Medical Systems, Inc.

Recalled Item: 10Fore Hemostasis Valve Catalog Number / UDI-DI code: MAPTEN4 / Recalled by...

The Issue: Due to a manufacturing issue involving the silicone quad ring where the ring...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2025· Olympus Corporation of the Americas

Recalled Item: Electrosurgical Recalled by Olympus Corporation of the Americas Due to...

The Issue: Potential for the ESG-410 Electrosurgical Generator to display an error...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2025· Olympus Corporation of the Americas

Recalled Item: Electrosurgical Recalled by Olympus Corporation of the Americas Due to...

The Issue: Potential for the ESG-410 Electrosurgical Generator to display an error...

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

Class II — Potential Health HazardOngoing
FoodJuly 24, 2025· Superior Foods Company

Recalled Item: Park Street Deli Cinnamon Bun Dessert Dip Net WT 7oz. Recalled by Superior...

The Issue: foreign material (plastic)

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2025· Cipla USA, Inc.

Recalled Item: Albuterol Sulfate Recalled by Cipla USA, Inc. Due to Failed Stability...

The Issue: Failed Stability Specifications: Out of specification results was observed...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 24, 2025· Dexcom, Inc.

Recalled Item: Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name:...

The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2025· Dexcom, Inc.

Recalled Item: Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name:...

The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2025· Dexcom, Inc.

Recalled Item: Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name:...

The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2025· Dexcom, Inc.

Recalled Item: Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name:...

The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2025· Dexcom, Inc.

Recalled Item: Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name:...

The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2025· THOR Photomedicine Ltd

Recalled Item: Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Recalled by THOR...

The Issue: The potential for a failed welded nut to shear off. When this occurs, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2025· Dentsply IH, Inc.

Recalled Item: Brand Name: Atlantis IO FLO Product Name: Atlantis IO FLO-S Recalled by...

The Issue: The defect in the thread area will not allow the device to fully engage with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2025· Dentsply IH, Inc.

Recalled Item: Brand Name: Atlantis IO FLO-S Product Name: Atlantis IO FLO-S Recalled by...

The Issue: The defect in the thread area will not allow the device to fully engage with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2025· THOR Photomedicine Ltd

Recalled Item: Brand Name: THOR Product Name: NovoTHOR XL Model/Catalog Number: S2190...

The Issue: The potential for a failed welded nut to shear off. When this occurs, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2025· THOR Photomedicine Ltd

Recalled Item: Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Recalled by THOR...

The Issue: The potential for a failed welded nut to shear off. When this occurs, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2025· THOR Photomedicine Ltd

Recalled Item: Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software...

The Issue: The potential for a failed welded nut to shear off. When this occurs, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2025· Boston Scientific Corporation

Recalled Item: ENDOTAK RELIANCE G/SG with 4-SITE Connector Recalled by Boston Scientific...

The Issue: Affected lead models may experience gradually rising LVSI measurements in...

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

Class I — Serious Health HazardOngoing