Product Recalls in Vermont

Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,541 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,541 in last 12 months

Showing 23412360 of 27,157 recalls

Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Welch Allyn Recalled by Baxter Healthcare Corporation Due to There is an...

The Issue: There is an issue with the ventilator battery charger that could lead to an...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Welch Allyn Recalled by Baxter Healthcare Corporation Due to There is an...

The Issue: There is an issue with the ventilator battery charger that could lead to an...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2024· New Medical Technologies Gmbh

Recalled Item: Integra Miltex Cryosolutions Cartridges 4 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· 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