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. 2,730 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,730 in last 12 months

Showing 1748117500 of 29,505 recalls

Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2017· Cyberonics, Inc

Recalled Item: VNS Therapy Programmer Recalled by Cyberonics, Inc Due to Certain Model 3000...

The Issue: Certain Model 3000 programming events can result in miscalculation of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump 3010 Series The Medfusion¿ Syringe Infusion Pumps...

The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump 3500 Series The Medfusion¿ Syringe Infusion Pumps...

The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump 4000 Series The Medfusion¿ Syringe Infusion Pumps...

The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2017· Amendia, Inc dba Spinal Elements

Recalled Item: Piranha Screw 4.0 x 12mm Recalled by Amendia, Inc dba Spinal Elements Due to...

The Issue: Potential incorrect marking and color identification of Piranha screw. Some...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution - Premixed Dialysate for Hemodialysis with...

The Issue: Using different fluid formulations of NxStage PureFlow B Solution at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Beckman Coulter Inc.

Recalled Item: iQ200 Series Urine Microscopy Analyzer with Barcode Reader Model NFT-2100...

The Issue: iQ200 Series Urine Microscopy Analyzer may intermittently fail to read urine...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· C.R. Bard, Inc.

Recalled Item: CritiCore Automated Urine Output and Temperature Monitor Recalled by C.R....

The Issue: Issues identified with the monitor including urine output measurement...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2017· Vascular Insights, LLC

Recalled Item: ClariVein IC infusion catheter Recalled by Vascular Insights, LLC Due to...

The Issue: Certain catheters could have a compromised catheter shaft due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista System LOCI 8 CALIBRATOR The LOCI 8 Calibrator Recalled by...

The Issue: An increase in the number of failed calibration events or negative bias with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2017· Bard Medical Division

Recalled Item: Medivance(R) ARCTIC SUN(R) ARCTICGEL(TM) Pads: Description Recalled by Bard...

The Issue: Specific lots of ArcticGel Pads have potential issues which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2017· Boston Scientific Corporation

Recalled Item: Innova Self-Expanding Stent System Recalled by Boston Scientific Corporation...

The Issue: Stent possibly unable to be fully released from the delivery system.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2017· Boston Scientific Corporation

Recalled Item: Innova Self-Expanding Stent System Recalled by Boston Scientific Corporation...

The Issue: Stent possibly unable to be fully released from the delivery system.

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

Class II — Potential Health HazardOngoing