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. 2,697 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,697 in last 12 months

Showing 1804118060 of 29,505 recalls

Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· R82 A/S

Recalled Item: Heron toilet and bath chair Model 880505-01 & 880505-11 Recalled by R82 A/S...

The Issue: Replacement campaign on all units that have a gas spring head in aluminum.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Curved Suction 90 9733451 EM ENT Recalled by Medtronic Navigation,...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: STERILE SAMPLE SORIN GROUP Recalled by Sorin Group USA, Inc. Due to...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Suction 9734308 Small AxiEM ENT Recalled by Medtronic Navigation,...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Spine Instrumentation Recalled by Medtronic Navigation, Inc. Due to...

The Issue: Potential for Spinal Clamps to be damaged when opened beyond intended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Spine Instrumentation Recalled by Medtronic Navigation, Inc. Due to...

The Issue: Potential for Spinal Clamps to be damaged when opened beyond intended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Spine Instrumentation Recalled by Medtronic Navigation, Inc. Due to...

The Issue: Potential for Spinal Clamps to be damaged when opened beyond intended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic ENT Prgm 9734636 Add Fusion Nav AxiEM Recalled by Medtronic...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Spine Instrumentation Recalled by Medtronic Navigation, Inc. Due to...

The Issue: Potential for Spinal Clamps to be damaged when opened beyond intended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Boston Scientific Corporation

Recalled Item: EMBLEM S-ICD Recalled by Boston Scientific Corporation Due to The device can...

The Issue: The device can deliver an atypical amount of energy due to memory corruption...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Boston Scientific Corporation

Recalled Item: EMBLEM MRI S-ICD Model 219 Recalled by Boston Scientific Corporation Due to...

The Issue: The device can deliver an atypical amount of energy due to memory corruption...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Spine Instrumentation Recalled by Medtronic Navigation, Inc. Due to...

The Issue: Potential for Spinal Clamps to be damaged when opened beyond intended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Boston Scientific Corporation

Recalled Item: SQ-RX 1010 Pulse Generator Recalled by Boston Scientific Corporation Due to...

The Issue: The device can deliver an atypical amount of energy due to memory corruption...

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

Class II — Potential Health HazardOngoing