Product Recalls in Connecticut

Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,587 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,587 in last 12 months

Showing 1160111620 of 28,245 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 26, 2020· Radiometer Medical ApS

Recalled Item: Blood gases (PCO2 Recalled by Radiometer Medical ApS Due to Potential risk...

The Issue: Potential risk of patient mix-up on analyzers due to software issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2020· Radiometer Medical ApS

Recalled Item: Blood gases (PCO2 Recalled by Radiometer Medical ApS Due to Potential risk...

The Issue: Potential risk of patient mix-up on analyzers due to software issues.

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