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 2826128280 of 29,505 recalls

Medical DeviceSeptember 28, 2012· ICU Medical, Inc.

Recalled Item: 3 PORT "OFF" MANIFOLD w/WASTE BAG Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical, Inc. has identified a potential comingling of components where...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Philips Medical System Extended Brilliance Workspace (EBW) Recalled by...

The Issue: Incorrect values may be displayed. Philips is issuing a software update...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· International Technidyne Corp.

Recalled Item: Pro Time Microcoagulation System/ Pro Time 3 Cuvette Recalled by...

The Issue: Some Pro Time3 Test Cuvettes within a specified lot range may recover lower...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· Encore Medical, Lp

Recalled Item: 6.5mm Cancellous Bone Screw Intended to be used for the Recalled by Encore...

The Issue: A product complaint was received where a size 20 screw was labeled as size...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2012· Cellestis Inc

Recalled Item: Vacuette Cellestis 1 ml QuantiFERON¿ TB ANTIGEN (HA) High Altitude: Shake...

The Issue: Cellestis is recalling QuantiFERON¿¿ - TB Gold TB Blood Collection Tubes and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2012· Cellestis Inc

Recalled Item: VACUETTE Cellestis 1 ml QuantiFERON¿ - TB ANTIGEN Recalled by Cellestis Inc...

The Issue: Cellestis is recalling QuantiFERON¿¿ - TB Gold TB Blood Collection Tubes and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2012· MOOG Medical Devices Group

Recalled Item: ***This recall is being conducted due to an incomplete recall Recalled by...

The Issue: This recall is the same issue for the FDA processed recall initiated by Moog...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Definium 5000/5220493-2 X-Ray System Recalled by GE...

The Issue: When quickly switching the protocols from AEC to Fixed under the same view,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2012· DeGotzen

Recalled Item: DeGotzen XRay unit XGenus Dental X-ray unit. Recalled by DeGotzen Due to It...

The Issue: It was discovered at the WEAC Labs method sample did not meet requirements...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Definium 5000 / 5220493 X-Ray System Recalled by GE...

The Issue: When quickly switching the protocols from AEC to Fixed under the same view,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing