Product Recalls in Georgia

Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,122 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
1,122 in last 12 months

Showing 13321–13340 of 29,505 recalls

Medical DeviceOctober 2, 2019· Zeiss, Carl Inc

Recalled Item: Component for Laser Scanning Microscopes (LSM 700 Recalled by Zeiss, Carl...

The Issue: When the user tilts the transmitted light arm of the microscope to the end...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. X-Port isp M.R.I Implantable Port Recalled by Bard Peripheral Vascular...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: BardPort M.R.I. Hard Base Implantable Port with Attachable 9.6 F Recalled by...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. Vaccess CT Power-Injectable Implantable Port with Suture Plugs Recalled...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: BardPort Titanium Implantable Port with Attachable 9.6 F Open-Ended...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: BardPort M.R.I. Implantable Port with Attachale 9.6 F Open-Ended...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: PowerFlow Implatable Apheresis IV Port with attachable 9.6 F ChronoFl...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. Groshong 9.5 Dual-Lumen CV Catheter Recalled by Bard Peripheral Vascular...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. Power Port isp M.R.I. Implantable Port with Attachable 9.6 Recalled by...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Rosie4 Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Accutorr 3 Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Rosebud Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Accutorr 7 Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Aesculap Implant Systems LLC

Recalled Item: Aesculap Sterile disposable fleece drape Recalled by Aesculap Implant...

The Issue: Packaging seal integrity not validated resulting in a lack of sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing