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. 2,686 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,686 in last 12 months

Showing 2088120900 of 29,505 recalls

Medical DeviceMay 17, 2016· X Spine Systems Inc

Recalled Item: Calix T PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...

The Issue: The trials and rasps used to prepare the surgical site for placement of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Comprehensive ventilator- Recalled by Carefusion 211 Inc dba Carefusion...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· CSL Behring GmbH

Recalled Item: Dimension Vista¿ Homocysteine Flex Reagent Cartridge (HCYS) Recalled by CSL...

The Issue: Reagent lots # 15243MA and 15243MB shows a reduced stability once opened...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2016· Ortho-Clinical Diagnostics

Recalled Item: enGen Laboratory Automation System Recalled by Ortho-Clinical Diagnostics...

The Issue: If the user selects the Comment or Interpretation option (in the enGEN .gsb...

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

Class III — Low RiskOngoing
Medical DeviceMay 16, 2016· FSC Laboratories, Inc

Recalled Item: Flexichamber Anti-Static Valved Collapsible Holding Chamber Recalled by FSC...

The Issue: Product had torn/loose seal around the mouthpiece.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2016· Lifeline First Aid LLC

Recalled Item: Item # 4042-CPR Rescue Kit Recalled by Lifeline First Aid LLC Due to First...

The Issue: First aid kits or rescue kits are recalled because they contains the CPR...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2016· Lifeline First Aid LLC

Recalled Item: 5195GM Recalled by Lifeline First Aid LLC Due to Cadillac First Aid Kit is...

The Issue: Cadillac First Aid Kit is recalled because it contains the CPR Shield with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2016· Medtronic Sofamor Danek Usa, Inc - Dallas Distribution

Recalled Item: Saw Sagittal Catalog Number: ES 300 Recalled by Medtronic Sofamor Danek Usa,...

The Issue: Medtronic Powered Surgical Solutions testing of the Sagittal Saw Rocker Arm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2016· Baxter Healthcare Corp

Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...

The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2016· Baxter Healthcare Corp

Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...

The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2016· CareFusion 303, Inc.

Recalled Item: Alaris System PC Unit Model 8015 with software versions 9.17 and 9.19...

The Issue: A patient weight can be populated incorrectly under certain conditions when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2016· Baxter Healthcare Corp

Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...

The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2016· Synthes (USA) Products LLC

Recalled Item: Norian Drillable Inject 3 CC-Sterile Recalled by Synthes (USA) Products LLC...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2016· Zimmer Biomet, Inc.

Recalled Item: Persona Trabecular Metal Tibia Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Zimmer Inc. is initiating a recall of specific Persona" Trabecular Metal"...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2016· Synthes (USA) Products LLC

Recalled Item: Norian Drillable Inject 5 CC-Sterile Recalled by Synthes (USA) Products LLC...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2016· Synthes (USA) Products LLC

Recalled Item: Norian Drillable Inject 10 CC-Sterile Recalled by Synthes (USA) Products LLC...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2016· Siemens Healthcare Diagnostics Inc.

Recalled Item: Hettich Centrifuge Modules: StreamLAB Centrifuge Module (10372372 or...

The Issue: Premature bucket failures

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2016· CarboFix Orthopedics, Ltd.

Recalled Item: Piccolo Composite Tibia and Femoral Nailing Systems - Ball Tip Recalled by...

The Issue: Firm received complaints where the Piccolo Composite Ball Tip Guide Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2016· Medical Vision Ab

Recalled Item: Double Pump RF Patient Cassette Recalled by Medical Vision Ab Due to...

The Issue: Sterility of device may be compromised due to sterile package breakage.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· Immuno-Mycologics, Inc

Recalled Item: Histoplasma Yeast Complement Fixation Antigen Dilute Ref# H30150 The fungal...

The Issue: The device was found to have bacterial contamination.

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

Class II — Potential Health HazardOngoing