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. 2,149 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,149 in last 12 months

Showing 35213540 of 29,505 recalls

Medical DeviceJuly 19, 2024· Inari Medical - Oak Canyon

Recalled Item: ClotTriever XL Catheter Recalled by Inari Medical - Oak Canyon Due to...

The Issue: Thrombectomy system catheter instructions for use updated to reduce adverse...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2024· Centinel Spine, Inc.

Recalled Item: prodisc C SK Recalled by Centinel Spine, Inc. Due to During the assembly of...

The Issue: During the assembly of Prodisc C, a blue discoloration was observed on a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2024· Centinel Spine, Inc.

Recalled Item: prodisc C SK Recalled by Centinel Spine, Inc. Due to During the assembly of...

The Issue: During the assembly of Prodisc C, a blue discoloration was observed on a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2024· Becton Dickinson & Co.

Recalled Item: BD BACTEC MGIT 960 PZA Kit)- IVD qualitative procedure for Recalled by...

The Issue: May intermittently produce falsely resistant results for pyrazinamide (PZA)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Mazor Robotics Ltd

Recalled Item: Mazor X. Model Number Recalled by Mazor Robotics Ltd Due to Software...

The Issue: Software anomalies which can result in two separate issues: A lagging screen...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Baxter Healthcare Corporation

Recalled Item: Spectrum Wireless Battery Modules A/B/G/N Recalled by Baxter Healthcare...

The Issue: The Spectrum WBM may fail to auto-document infusion status information back...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Beckman Coulter Biomedical GmbH

Recalled Item: PE Centrifuge Recalled by Beckman Coulter Biomedical GmbH Due to The...

The Issue: The adhesive joint between the plastic socket and metal component of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Boston Scientific Neuromodulation Corporation

Recalled Item: WAVEWRITER ALPHA: Model: SC-1216 Recalled by Boston Scientific...

The Issue: Spinal Cord Stimulation (SCS) Implantable Pulse Generator (IPG) may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter Spectrum Wireless Battery Modules A/B/G/N Recalled by Baxter...

The Issue: The Spectrum WBM may fail to auto-document infusion status information back...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Beckman Coulter Biomedical GmbH

Recalled Item: PE Centrifuge Temperature Controlled Recalled by Beckman Coulter Biomedical...

The Issue: The adhesive joint between the plastic socket and metal component of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Beckman Coulter Biomedical GmbH

Recalled Item: Power Express Recalled by Beckman Coulter Biomedical GmbH Due to The...

The Issue: The adhesive joint between the plastic socket and metal component of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...

The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 16, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo...

The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 16, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Firm has released a...

The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: 25+ CMB PAK 10K CPM Recalled by Alcon Research LLC Due to...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: Alcon Custom Pak Model/Catalog Number: Many Software Version:...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Recalled by...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT SATINSLIT FULL HANDLE3.0MM ANG...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: 25+ TOTALPLUSr CP PAK 20K CPM BWV .9 Recalled by Alcon...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: 25+ CMB PAK 10K CPM Recalled by Alcon Research LLC Due to...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing