Product Recalls in New Mexico

Product recalls affecting New Mexico — including food, drugs, consumer products, medical devices, and vehicles distributed to New Mexico. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,606 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
2,606 in last 12 months

Showing 12211240 of 27,850 recalls

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
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
Medical DeviceJuly 24, 2025· Boston Scientific Corporation

Recalled Item: RELIANCE 4-FRONT Recalled by Boston Scientific Corporation Due to Affected...

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
Medical DeviceJuly 24, 2025· Boston Scientific Corporation

Recalled Item: ENDOTAK RELIANCE G/SG Recalled by Boston Scientific Corporation Due to...

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
Medical DeviceJuly 22, 2025· Physio-Control, Inc.

Recalled Item: LIFEPAK CR2 Part / Catalog Numbers / UDI-DI code: CR2-2-001451 Recalled by...

The Issue: Due to required inspections not being performed on products/units that have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2025· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 Recalled by...

The Issue: Due to required inspections not being performed on products/units that have...

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

Class II — Potential Health HazardOngoing