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 23212340 of 27,157 recalls

Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx15mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 8mmx8mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 8mmx8mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx15mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Delivery System 15mmx10mm UPN: M00553750 Recalled by Boston...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN:...

The Issue: Reported Outer sheath distal black tip detaching from the device can remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter Continu-Flo Solution Set with Duo-Vent Spike Recalled by Baxter...

The Issue: Specific lots of Solution Sets with Duo-Vent Spike have the potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Randox Laboratories, Limited

Recalled Item: Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Recalled by Randox...

The Issue: Lipoprotein (a) on Roche Cobas c501 with nmol/l claims does not have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Randox Laboratories, Limited

Recalled Item: Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Recalled by Randox...

The Issue: Lipoprotein (a) on Roche Cobas c501 with nmol/l claims does not have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter Solution Set with Duo-Vent Spike Recalled by Baxter Healthcare...

The Issue: Specific lots of Solution Sets with Duo-Vent Spike have the potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter Clearlink System Solution Set with Duo-Vent Spike Recalled by Baxter...

The Issue: Specific lots of Solution Sets with Duo-Vent Spike have the potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Integrity Implants Inc.

Recalled Item: Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number:...

The Issue: Due to incompatibility of bone tamp (Rev A) and bone funnels (Rev C).

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

Class II — Potential 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 20, 2024· Baxter Healthcare Corporation

Recalled Item: Breathe Technologies Recalled by Baxter Healthcare Corporation Due to There...

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