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. 2,793 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,793 in last 12 months

Showing 1092110940 of 29,505 recalls

Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus LS - Manual Defibrillator Recalled by Remote Diagnostic Technologies...

The Issue: A software error was detected within software version 1.3.4 for the Tempus...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2020· Zimmer Biomet, Inc.

Recalled Item: Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System Recalled by...

The Issue: Zimmer Biomet is conducting a medical device correction to update the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2020· Boston Scientific Corporation

Recalled Item: Contour VL Variable Length Ureteral Stent Set Recalled by Boston Scientific...

The Issue: Trace amounts of metallic debris were found on the stent related to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2020· Boston Scientific Corporation

Recalled Item: Contour VL Variable Length Ureteral Stent Recalled by Boston Scientific...

The Issue: Trace amounts of metallic debris were found on the stent related to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2020· Galt Medical Corporation

Recalled Item: Centeze Centesis Catheter Recalled by Galt Medical Corporation Due to Due to...

The Issue: Due to a manufacturing issue, the catheter tip geometry is incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2020· Covidien Llc

Recalled Item: Capnostream 35 Portable Respiratory Monitor Recalled by Covidien Llc Due to...

The Issue: The firm has released software update V01.05.02.16 (also known as V1.5.2) in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2020· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic Cobalt DR MRI SureScan DDPB3D1 Recalled by Medtronic Inc., Cardiac...

The Issue: Under rare circumstances, the component may be susceptible to a failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2020· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic Cobalt HF CRT-D MRI SureScan DTPB2D1 Recalled by Medtronic Inc.,...

The Issue: Under rare circumstances, the component may be susceptible to a failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2020· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic COBALT HF QUAD CRT-D MRI SureScan Recalled by Medtronic Inc.,...

The Issue: Under rare circumstances, the component may be susceptible to a failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2020· Randox Laboratories Ltd.

Recalled Item: Randox Mg R1 - Product Usage: For the quantitative in Recalled by Randox...

The Issue: Failing to meet the linearity performance claims quoted on the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2020· Randox Laboratories Ltd.

Recalled Item: Randox Rx Series Mg - Product Usage: For the quantitative Recalled by Randox...

The Issue: Failing to meet the linearity performance claims quoted on the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2020· Medtronic Inc.

Recalled Item: CareLink Personal Software Therapy Management Software Tool for Diabetes...

The Issue: Incomplete basal rate information may be transmitted leading to a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2020· Medtronic Neuromodulation

Recalled Item: Medtronic Intellis Spinal Cord Stimulator Recalled by Medtronic...

The Issue: A710 Intellis Clinician Application has a software issue that can result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2020· ConMed Corporation

Recalled Item: Infinity ACL Tibial Tip Guide- indicated for use in open Recalled by ConMed...

The Issue: Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2020· ConMed Corporation

Recalled Item: Infinity ACL Tibial Elbow Guide-indicated for use in open and Recalled by...

The Issue: Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2020· Biocomposites, Ltd.

Recalled Item: Stimulan Kit 10cc Recalled by Biocomposites, Ltd. Due to Mislabeling

The Issue: The product is mislabeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2020· Hill-Rom Manufacturing, Inc.

Recalled Item: Life2000 Ventilation System Recalled by Hill-Rom Manufacturing, Inc. Due to...

The Issue: Under certain conditions, there is a risk for fire.

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

Class II — Potential Health HazardOngoing