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. 2,313 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,313 in last 12 months

Showing 3272132740 of 47,027 recalls

Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Knee Undersleeve Gray Product Usage: Knee undersleeves are worn as Recalled...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: syngo X Workplace is a medical workstation for real-time viewing Recalled by...

The Issue: After importing, the segmentation results appear mirrored at the CARTO...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Rebound Cartilage Product Usage: Rebound Cartilage is an external knee...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Rebound Air Walker Product Usage: Rebound Air Walkers are indicated Recalled...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Papoose Infant Spine Immobilizer Item # Item Description: PA-100 Papoose...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Rebound Cartilage Custom Product Usage: Rebound Cartilage Custom is an...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Unloader Custom Lite Product Usage: Unloader Custom Lite is an Recalled by...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Rebound Diabetic Walker Product Usage: Rebound Diabetic Walkers are used...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup Recalled by...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G4 PLATINUM Receiver with Share Receiver Part Number: MT22495...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2016· Synthes (USA) Products LLC

Recalled Item: Titanium Low Profile Neuro Screw Recalled by Synthes (USA) Products LLC Due...

The Issue: Out of specification at the thread. The thread height of these screws is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Custom Tubing Packs Custom tubing pack for oxygenators Recalled by Maquet...

The Issue: Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Maquet Cardiovascular Us Sales, Llc

Recalled Item: HLS Set Advanced with BIOLINE Coating Custom tubing packs for the oxygenator...

The Issue: Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G4 PLATINUM (Pediatric) Receiver with Share Receiver Part Number:...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2016· Maquet Cardiovascular Us Sales, Llc

Recalled Item: QUADROX-i oxygenators Custom tubing packs for the oxygenator Recalled by...

The Issue: Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Medtronic Inc.

Recalled Item: Reveal LINQ insertable Cardiac Monitor Recalled by Medtronic Inc. Due to...

The Issue: Medtronic has identified an issue with the sensitivity of an algorithm used...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G5 Mobile Receiver Receiver Part Number: MT22719 Receiver (mg/dL)...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G4 PLATINUM Receiver Receiver Part Number: MT20649 Receiver (mg/dL)...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2016· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Rotaflow Centrifugal Pump Custom tubing packs for the oxygenator Recalled by...

The Issue: Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G4 PLATINUM (Pediatric) Receiver Receiver Part Number: MT22430...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

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

Class I — Serious Health HazardOngoing