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 2752127540 of 53,623 recalls

Medical DeviceJune 21, 2018· Becton Dickinson & Co.

Recalled Item: BD BBL GC-Lect Agar Recalled by Becton Dickinson & Co. Due to A portion of...

The Issue: A portion of this lot was manufactured using Gentamicin instead of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust Escudo D144DRG (OUS distribution) Product Usage: The...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature sensing catheter 16FR Recalled by Degania Silicone, Ltd. Due to...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Foley Catheter with temperature sensor 400TM 8FR Recalled by Degania...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· DePuy Orthopaedics, Inc.

Recalled Item: CORAIL Cementless Femoral Stem HA Coated Standard Size 11 Recalled by DePuy...

The Issue: Two lots of femoral stems were labeled as Size 11. However, they are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Thermistor Foley catheter Recalled by Degania Silicone, Ltd. Due to The...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust Escudo D144VRC (OUS distribution) Product Usage: The...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature Sensor Catheter 18FR Recalled by Degania Silicone, Ltd. Due to...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Johnson & Johnson Surgical Vision Inc

Recalled Item: Abbott TECNIS 1-Piece Aspheric Acrylic IOL with the TECNIS iTEC Recalled by...

The Issue: Expired intraocular lenses were distributed.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...

The Issue: The flow rate test verification was not properly executed for certain Sigma...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Foley Catheter with temperature sensor 400TM 16FR Recalled by Degania...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature Sensor Catheter 10FR Recalled by Degania Silicone, Ltd. Due to...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature sensing catheter 14FR Recalled by Degania Silicone, Ltd. Due to...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing