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 2144121460 of 29,505 recalls

Medical DeviceFebruary 23, 2016· Medtronic Inc.

Recalled Item: Reveal LINQ insertable Cardiac Monitor Recalled by Medtronic Inc. Due to...

The Issue: Medtronic has identified an issue with the sensitivity of an algorithm used...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G5 Mobile Receiver Receiver Part Number: MT22719 Receiver (mg/dL)...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G4 PLATINUM (Pediatric) Receiver Receiver Part Number: MT22430...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2016· Dexcom Inc

Recalled Item: Dexcom G4 PLATINUM (Professional) Receiver Receiver Part Number: MT20649...

The Issue: Customers may not receive an intended audible alarm or alert if relying on...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas p 512 pre-analytical system Pre-analytical sample handling that...

The Issue: Due to a false triggering or detection of the lifting gripper READY signal,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Synthes (USA) Products LLC

Recalled Item: Titanium Low Profile Neuro Screw Recalled by Synthes (USA) Products LLC Due...

The Issue: Out of specification at the thread. The thread height of these screws is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2016· Synthes (USA) Products LLC

Recalled Item: Titanium Low Profile Neuro Screw Recalled by Synthes (USA) Products LLC Due...

The Issue: Out of specification at the thread. The thread height of these screws is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2016· Pentax Medical Company

Recalled Item: Video Duodenoscope Recalled by Pentax Medical Company Due to Pentax Medical...

The Issue: Pentax Medical learned of reports of carbapenem-resistant Enterobacteriaceae...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2016· Innovative Ophthalmic Products, Inc

Recalled Item: Molteno3 Glaucoma Implants G-Series: GS-Single Plate 175mm2 (IOP reorder#:...

The Issue: Innovative Ophthalmic Products (IOP) is recalling the Molteno 3 G-Series...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software issues on Cios Alpha mobile C-Arm system

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis (system Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Possible leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego (system Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Possible leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Horiba Instruments Inc

Recalled Item: ABX Pentra 400 (version 5.0.8 or lower) The ABX PENTRA Recalled by Horiba...

The Issue: Horiba Instruments, Inc. is recalling ABX Pentra 400( version 5.0.8 or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Horiba Instruments Inc

Recalled Item: Pentra C400 (version 1.1.2 or lower) The ABX PENTRA 400 Recalled by Horiba...

The Issue: Horiba Instruments, Inc. is recalling ABX Pentra 400( version 5.0.8 or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Integrated Science Systems Inc

Recalled Item: Sure Vue Color Staph 150T Recalled by Integrated Science Systems Inc Due to...

The Issue: Customer complaints of very weak reactions with the kit, or false negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· TEM Systems Inc

Recalled Item: ROTROL P Control for ROTEM delta Thromboelastometry System Recalled by TEM...

The Issue: Customer complaints about failed target ranges for alpha angle. Firm has not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing