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. 2,621 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,621 in last 12 months

Showing 3438134400 of 53,623 recalls

Medical DeviceSeptember 29, 2016· Sorin Group USA, Inc.

Recalled Item: The ORCHESTRA PLUS Programmer A portable device Recalled by Sorin Group USA,...

The Issue: Sorin Group USA, Inc. announces a voluntary field action for the ORCHESTRA...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: FlexLab Automation Modules Recalled by Siemens Healthcare Diagnostics, Inc....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Thayer Medical Corporation

Recalled Item: Thayer MiniSpacer Dual Spray MDI Adapter Counter Incrementing Actuator with...

The Issue: The insert and case label description of the device incorrectly reads...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· SentreHeart Inc

Recalled Item: FindrWIRZ Guidewire System Catalog# 40-05 Cardiology: The system is intended...

The Issue: A complaint was received on September 27th, 2016 at a medical center in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 29, 2016· Mako Surgical Corporation

Recalled Item: Stryker Restoris RIO Reamer Handle Recalled by Mako Surgical Corporation Due...

The Issue: Failure of the Offset Cup Reamer Handle not engaging its mating components.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Aptio Automation Modules Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Possible overheating of power cord plugs used to connect to FlexLab and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Covidien LLC

Recalled Item: Covidien Devon Light Glove packaged in sterile surgical kits : Recalled by...

The Issue: Added Instructions for Use: After application, inspect the Light Glove for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Sorin Group USA, Inc.

Recalled Item: The ORCHESTRA Programmer A portable device Recalled by Sorin Group USA, Inc....

The Issue: Sorin Group USA, Inc. announces a voluntary field action for the ORCHESTRA...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Baxter Healthcare Corp.

Recalled Item: Baxter SIGMA Spectrum INFUSION PUMP with Master Drug Library Recalled by...

The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Baxter Healthcare Corp.

Recalled Item: sigma spectrum VOLUMETRIC INFUSION PUMP with Master Drug Library Recalled by...

The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Zimmer Biomet, Inc.

Recalled Item: Zimmer¿ Gender Solutions" Patellofemoral Joint Prosthesis Milling Handpiece...

The Issue: Complaints have been reported that the handpiece is inoperable. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Baxter Healthcare Corp.

Recalled Item: V6 Rear Case Assembly Recalled by Baxter Healthcare Corp. Due to A...

The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS 4F Stiffened Micro-Introducer Recalled by Angiodynamics, Inc....

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
FoodSeptember 28, 2016· Brownwood Farms

Recalled Item: Brownwood Farms BBQ Mustard Glaze. 11oz glass bottles and 1 Recalled by...

The Issue: Products contain soy ingredients not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund