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. 2,485 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,485 in last 12 months

Showing 1778117800 of 28,245 recalls

Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Z NAIL PF 14MM X 46CM UNIV Z NAIL GT Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: FEM IM NAIL 15MMDX30CM Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: FEM IM NAIL 14MMDX30CM LEFT Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: VERSA-FXII SC TUBE PLT 90DX16H Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: TI Transport Monitor/Module Battery Pack Product Usage: intended for...

The Issue: Mindray has received two reports from outside the United States that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing