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. 2,605 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
2,605 in last 12 months

Showing 34213440 of 48,595 recalls

Medical DeviceDecember 19, 2024· New Medical Technologies Gmbh

Recalled Item: Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each) Recalled by...

The Issue: During the assembly of the cartridge to its connecting body part, the valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Becton Dickinson & Co.

Recalled Item: BD PCR Cartridges used with MAX System. Model Number: 437519 Recalled by...

The Issue: Potential for signal drift in specific lots of BD PCR Cartridges.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Ortho-Clinical Diagnostics, INc.

Recalled Item: Brand Name: VITROS Product Name: VITROS XT 7600 Integrated System Recalled...

The Issue: The VITROS XT 7600 Integrated System software versions 3.8.0 may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Ortho-Clinical Diagnostics, INc.

Recalled Item: Brand Name: VITROS Product Name: VITROS 5600 Integrated System Model/Catalog...

The Issue: The VITROS 5600 Integrated System software versions 3.8.0 may not correctly...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Ortho-Clinical Diagnostics, INc.

Recalled Item: Brand Name: VITROS Product Name: VITROS 3600 Immunodiagnostic System...

The Issue: The VITROS 3600 Immunodiagnostic System software versions 3.8.0 may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Jinan Bodor Cnc Machine Co Ltd

Recalled Item: Bodor P and C series laser cutting machines Recalled by Jinan Bodor Cnc...

The Issue: Non-compliant laser products

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

Class II — Potential Health HazardOngoing