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 2192121940 of 53,623 recalls

Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/wing (2264LAX)...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Ra Medical Systems, Inc.

Recalled Item: Ra Medical Systems DABRA Catheter 5F (1.5mm) Recalled by Ra Medical Systems,...

The Issue: The firm has become aware there is a potential problem with its DABRA...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Recalled by Pacific...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob Recalled by...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical Philips M1355A Toco Transducer with belt wire/knob Recalled...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Baxter Healthcare Corporation

Recalled Item: TherMax Blood Warmer Unit Recalled by Baxter Healthcare Corporation Due to...

The Issue: TherMax Blood Warmers may not be in compliance with an electrical safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Xodus Medical Inc

Recalled Item: Cautery Tip Cleaner Product Usage: electrosurgical accessory Recalled by...

The Issue: The sterile barrier of some devices may have been affected

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Xodus Medical Inc

Recalled Item: Electrosurgical Tip Cleaner Product Usage: electrosurgical accessory...

The Issue: The sterile barrier of some devices may have been affected

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· CrossRoads Extremity Systems, LLC

Recalled Item: MotoBand CP Recalled by CrossRoads Extremity Systems, LLC Due to Potentially...

The Issue: Potentially includes a 3.0mm x 30mm screw instead of 3.0mm x 28mm screw.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Xodus Medical Inc

Recalled Item: Electrosurgical Tip Cleaner Product Usage: electrosurgical accessory...

The Issue: The sterile barrier of some devices may have been affected

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2019· Senseonics, Inc.

Recalled Item: Eversense CGM SENSOR (FG-4200-00-301)-Continuous Glucose Monitor Recalled by...

The Issue: Eversense Sensors have prematurely stopped functioning due to inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: XCELA Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due to Snap...

The Issue: Snap lock connectors provided within implantable port kits may not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BIOFLO 8F SINGLE PLASTIC NON-FILLED Recalled by Angiodynamics Inc. (Navilyst...

The Issue: Snap lock connectors provided within implantable port kits may not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2019· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the Recalled by...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2019· Biomedical Polymers, Inc.

Recalled Item: Hemo-Drop Blood Dispenser Recalled by Biomedical Polymers, Inc. Due to The...

The Issue: The metal cannula of the device either broke and the broken piece left in...

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

Class III — Low RiskOngoing