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 2596125980 of 29,505 recalls

Medical DeviceDecember 20, 2013· Perrigo Diabetes Care

Recalled Item: Orbit soft Infusion sets Recalled by Perrigo Diabetes Care Due to Perrigo...

The Issue: Perrigo was notified by our supplier, Ypsomed AG, that they are recalling...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· Optimedica Corporation

Recalled Item: Catalys Precision Laser System (United States) - Catalys-U: Catalys...

The Issue: Potential for unexpected heating of the transformer mounting bolt located...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Single and Dual use Emission Computer Tomography gamma cameras (BrightView...

The Issue: Three problems were reported to the firm: When positioning for a relative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Spacelabs Healthcare, Llc

Recalled Item: ARIATELE TELEMETRY TRANSMITTER Recalled by Spacelabs Healthcare, Llc Due to...

The Issue: The AriaTele Model 96281 with SpO2 monitoring Option C is recalled because...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Biomet, Inc.

Recalled Item: Locking Cortical Screw 3.5mmX38mm Recalled by Biomet, Inc. Due to 3.5mmx38mm...

The Issue: 3.5mmx38mm Locking Cortical Screw, implants are being recalled since an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· ITC-Nexus Dx

Recalled Item: Hemochron Jr. Citrate APTT Cuvette 510(k) K014008 A unitized...

The Issue: ITC has determined that some Citrate APTT cuvettes may recover higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Teleflex Medical

Recalled Item: Weck Recalled by Teleflex Medical Due to Sterility cannot be guaranteed.

The Issue: Sterility cannot be guaranteed.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Zimmer, Inc.

Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...

The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Zimmer, Inc.

Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...

The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray...

The Issue: During internal testing, the Brilliance CT Big Bore was found to be out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Teleflex Medical

Recalled Item: Weck Recalled by Teleflex Medical Due to Sterility cannot be guaranteed.

The Issue: Sterility cannot be guaranteed.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Steris Corporation

Recalled Item: VERIFY¿ SixCess 270FP Challenge Pack Recalled by Steris Corporation Due to...

The Issue: STERIS has identified that the outer shipping package for one lot (Lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ Systems Phenytoin Calibrator N ( PHTN) 6-pack SMN Recalled by...

The Issue: ADVIA Centaur¿ Systems Phenytoin Calibrator N, lots CN58 and higher, change...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ Systems Phenytoin Calibrator N ( PHTN) 2-pack SMN Recalled by...

The Issue: ADVIA Centaur¿ Systems Phenytoin Calibrator N, lots CN58 and higher, change...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA Urine Control L/H. The ABX PENTRA Urine Control Recalled by...

The Issue: HORIBA Medical is informing all ABX PENTRA Urine Control L/H customers...

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

Class III — Low RiskOngoing
Medical DeviceDecember 18, 2013· Merit Medical Systems, Inc.

Recalled Item: Radial Assist RAD BOARD Recalled by Merit Medical Systems, Inc. Due to Merit...

The Issue: Merit Medical Systems, Inc. is voluntarily recalling one lot (B507171) of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 12-15 mm...

The Issue: Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Stryker Spine

Recalled Item: Specialty Straight Static Inserter Assembly Product Usage: This instrument...

The Issue: Stryker has received complaints from customers relating to fracture along...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 9-12 mm...

The Issue: Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 12-15 mm...

The Issue: Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive...

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

Class II — Potential Health HazardOngoing