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. 2,673 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,673 in last 12 months

Showing 2126121280 of 29,505 recalls

Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Computed Tomography X-ray systems is intended to produce...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Siemens Healthcare Diagnostics Inc.

Recalled Item: Dimension Vista 500 Intelligent Lab System running on software versions...

The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Siemens Healthcare Diagnostics Inc.

Recalled Item: Dimension Vista 1500 Intelligent Lab System running on software versions...

The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance BigBore Oncology Computed Tomography X-ray systems Recalled by...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray systems is intended to produce...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems is intended to Recalled...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Teleflex Medical

Recalled Item: Weck EFx Classic Fascial Closure System Recalled by Teleflex Medical Due to...

The Issue: Incorrect expiration date was printed on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Abbott Laboratories

Recalled Item: CELL-DYN Emerald Cleaner Recalled by Abbott Laboratories Due to Three lots...

The Issue: Three lots of CELL-DYN Emerald Cleaner may have occurrences where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance BigBore Radiology Computed Tomography X-ray systems Recalled by...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2016· Acumedia Manufacturers, Inc.

Recalled Item: Nutrient Gelatin Recalled by Acumedia Manufacturers, Inc. Due to Incorrect...

The Issue: Incorrect expiration date was listed on the label. Correct expiration date...

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

Class III — Low RiskOngoing
Medical DeviceMarch 22, 2016· Medscience Inc

Recalled Item: AllergiEnd ST-9 Multiple Skin Test Applicator (Item 1000) and AllergiEnd...

The Issue: During an FDA inspection it was found that the products are marketed without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2016· Coloplast Manufacturing US, LLC

Recalled Item: Self-Cath¿ Pediatric Catheter Size CH 06 Recalled by Coloplast Manufacturing...

The Issue: Coloplast Corp. is voluntarily recalling a single lot of Self-Cath Pediatric...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2016· Leica Microsystems, Inc.

Recalled Item: Novocastra Liquid Mouse Monoclonal Antibody Calretinin Recalled by Leica...

The Issue: Novocastra Liquid Mouse Monoclonal Antibody Calretinin when used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2016· Boston Scientific Corporation

Recalled Item: Boston Scientific Fetch 2 Aspiration Catheter Recalled by Boston Scientific...

The Issue: Boston Scientific is recalling all models of Fetch 2 Aspiration Catheter as...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2016· Windstone Medical Packaging, Inc.

Recalled Item: General Surgery Pack Recalled by Windstone Medical Packaging, Inc. Due to...

The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Stryker Neurovascular

Recalled Item: GDC-18 360 11MM X 30CM Detachable Coil Sterile Recalled by Stryker...

The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioVac Circuit Pack (Tandem Packs) Recalled by Angiodynamics Inc....

The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Windstone Medical Packaging, Inc.

Recalled Item: Laparotomy Pack Latex Free Recalled by Windstone Medical Packaging, Inc. Due...

The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Vortex MEDICAL AngioVac Circuit Recalled by Angiodynamics Inc. (Navilyst...

The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Windstone Medical Packaging, Inc.

Recalled Item: Laparotomy Pack Recalled by Windstone Medical Packaging, Inc. Due to These...

The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...

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

Class II — Potential Health HazardOngoing