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 2198122000 of 29,505 recalls

Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: Anesthesia device service kits. ASSY-MSN Recalled by GE Medical Systems, LLC...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and...

The Issue: The door latch may not fully close and the door may open unexpectedly. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Bio-Rad Laboratories, Inc.

Recalled Item: D-10 Rack Loader Recalled by Bio-Rad Laboratories, Inc. Due to On a rare...

The Issue: On a rare occasion, there is a potential to assign a patient result to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Globalmed Logistix

Recalled Item: Lipogems SPA Aspiration Cannulae Recalled by Globalmed Logistix Due to The...

The Issue: The cannulae may bend during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A Recalled...

The Issue: An issue with the Panorama Central Station may cause the system to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2015· Becton, Dickinson and Company, BD Biosciences

Recalled Item: FMC7 FITC Recalled by Becton, Dickinson and Company, BD Biosciences Due to...

The Issue: Becton, Dickinson and Company (BD) has determined that the FMC7 FITC (ASR)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 11, 2015· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI¿ H/S Cuvette The intended use for the CDI¿ H Recalled by Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received complaints of the...

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

Class III — Low RiskOngoing
Medical DeviceDecember 11, 2015· Benlan, Inc.

Recalled Item: MED-RX Single Use Recalled by Benlan, Inc. Due to The product may be...

The Issue: The product may be packaged with a 5 or 6.5FR tube instead of an 8FR size.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Flow-i Anesthesia System Product Usage: The indication for the Flow-i...

The Issue: Electrical issues in the control, monitoring or panel sub-systems, caused by...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 10, 2015· Iba Dosimetry Gmbh

Recalled Item: IBA Dosimetry GmbH Lift Table Type 4320 Recalled by Iba Dosimetry Gmbh Due...

The Issue: When the electric lift table is connected to the mains power, in a very rare...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2015· Zimmer Biomet, Inc.

Recalled Item: Zimmer Periarticular Locking Plate System 3.5mm Locking Screw 58 mm Length...

The Issue: Product on the package label did not match what was inside the package. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2015· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System MOSAIQ is an oncology information system...

The Issue: Incorrect drug dosage due to "Age Limit" and patient weight data item issue.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer ClWIZARD2 5-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 2-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing