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. 2,471 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,471 in last 12 months

Showing 1140111420 of 27,157 recalls

Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Safe-T-Centesis 6 Fr Catheter Drainage Tray w/o Lidocaine Recalled by...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Safe-T-Centesis 8 Fr Catheter Drainage Tray Recalled by Carefusion 2200 Inc...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Safe-T PLUS Thora-Para 5 Fr Non-Valved Catheter Drainage Tray Recalled by...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Safe-T-Centesis PLUS 6 Fr Catheter Drainage Tray Recalled by Carefusion 2200...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Thora-Para 8 Fr Catheter Drainage Tray w/o Lidocaine Recalled by Carefusion...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Safe-T-Centesis 6 Fr Catheter Drainage Tray Recalled by Carefusion 2200 Inc...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Thora-Para 8 Fr Catheter Drainage Tray Recalled by Carefusion 2200 Inc Due...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Safe-T 5 Fr Thora-Para Tray With 5 Fr. Catheter and Recalled by Carefusion...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Safe-T 8 Fr Thora-Para Tray With 8 Fr. Catheter and Recalled by Carefusion...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2020· Carefusion 2200 Inc

Recalled Item: Thora-Para 5 Fr Non-Valved Catheter Drainage Tray Recalled by Carefusion...

The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath Paediatric catheters for blind protected distal bronchial...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath catheters for blind or fibrescope-guided protected distal...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath Paediatric catheters for blind protected distal bronchial...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2020· Prodimed Plastimed Division

Recalled Item: Prodimed Combicath catheters for blind or fibrescope-guided protected distal...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2020· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Synapse PACS Software Version 5.5.x and 5.7.x- intended as Recalled...

The Issue: Lateromedial (LM) and Lateromedial Oblique (LMO) Orientation Markers may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2020· Tosoh Bioscience Inc

Recalled Item: AIA-900 Analyzer Recalled by Tosoh Bioscience Inc Due to The Substrate...

The Issue: The Substrate Monitoring System in the AIA-900 Analyzer did not detect an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2020· Vitalconnect Inc.

Recalled Item: VistaSolution Recalled by Vitalconnect Inc. Due to A healthcare provider...

The Issue: A healthcare provider (HCP) noticed a patient had a lowered historic SpO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System Software Versions 3.3.3 and below...

The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...

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

Class II — Potential Health HazardOngoing