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. 2,661 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,661 in last 12 months

Showing 2234122360 of 29,505 recalls

Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD10 Recalled by Philips Electronics North America Corporation...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD20 Recalled by Philips Electronics North America Corporation...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 15-12 (biplane) Recalled by Philips Electronics North...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT HOLYOKE HOSPITAL SPECIAL PROCEDURE KIT Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: INTEGRIS V3000 Recalled by Philips Electronics North America Corporation Due...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· St Jude Medical Cardiac Rhythm Management Division

Recalled Item: Optisure Dual Coil Defibrillation Leads Recalled by St Jude Medical Cardiac...

The Issue: Leads may have been compromised during the manufacturing process, with cuts...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Cardiovascular Allura Centron Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD20 Biplane OR Table Recalled by Philips Electronics North...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: INTEGRIS BH3000 Recalled by Philips Electronics North America Corporation...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 9 (biplane) Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: UNIQ FD OR table Recalled by Philips Electronics North America Corporation...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: UNIQ FD Recalled by Philips Electronics North America Corporation Due to The...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD20/20 Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD20/15 Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD10 OR Table Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD20 Biplane Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: INTEGRIS BN/BV3000 Recalled by Philips Electronics North America Corporation...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT RENOWN REGIONAL MEDICAL CENTER Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD10/10 Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing