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. 2,643 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,643 in last 12 months

Showing 2598126000 of 29,505 recalls

Medical DeviceDecember 18, 2013· Zimmer Biomet, Inc.

Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...

The Issue: Possible break in the connector of the Force Sensor.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens ADVIA 1200 and ADVIA 1650 Chemistry Systems. Automated Recalled by...

The Issue: An overflow flag //// is displayed in the result column for a test when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Bicarbonate Jug Adapter to the 2008 Series Hemodialysis machine...

The Issue: Bicarbonate Jug Adapter distributed prior to 510(k) approval

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Carbide Cutting Burrs & Drums: 2MM Carbide Fluted Ball Recalled by...

The Issue: Some carbide cutting burr fractured during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Carbide Cutting Burrs: 1.5MMx7.5MM Cylindrical Carbide Drum part #...

The Issue: Some carbide cutting burr fractured during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Carbide Cutting Burrs & Drums: 1.5MM x 7.5MM Cylindrical Recalled by...

The Issue: Some carbide cutting burr fractured during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Carbide Cutting Burrs: 2MM Carbide Fluted Ball Recalled by The...

The Issue: Some carbide cutting burr fractured during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· Advanced Sterilization Products

Recalled Item: STERRAD NX Sterilization System Recalled by Advanced Sterilization Products...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 100S Sterilization System Recalled by Advanced Sterilization...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· Covidien

Recalled Item: Puritan Bennett 840 ventilator systems software part number 4-070212-85...

The Issue: Covidien is conducting a voluntary field corrective action on Puritan...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 16, 2013· GE Healthcare, LLC

Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...

The Issue: GE Healthcare has recently become aware of a potential safety issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis zee Ceiling Systems. Angiographic x-ray system. Recalled by...

The Issue: During the lifetime of Artis zee Ceiling systems, there is an increased wear...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 50 Sterilization System Recalled by Advanced Sterilization Products...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2013· Codman & Shurtleff, Inc.

Recalled Item: CODMAN CERTAS Programmable Valves Recalled by Codman & Shurtleff, Inc. Due...

The Issue: Ensuring all customers have the tools to assist in verifying the setting of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Upgrade Kit Recalled by GE Healthcare Due to Medical device adjustment knob...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System Recalled by Terumo...

The Issue: Sterility of medical devices intended for use in surgical procedures may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Panda iRes¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Giraffe¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing