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. 2,786 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,786 in last 12 months

Showing 1240112420 of 29,505 recalls

Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart pump is assembled into kits: TandemLife Kit Product: 5740-0000...

The Issue: Failure to prime due to an assembly error

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart pump is assembled into kits: ProtekDuo Kit - DL31 RD Recalled by...

The Issue: Failure to prime due to an assembly error

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A15 Recalled...

The Issue: Failure to prime due to an assembly error

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2020· Philips North America, LLC

Recalled Item: TRx4841A 1.4 GHz IntelliVue Tele TRX Recalled by Philips North America, LLC...

The Issue: The ECG signal from patients being monitored using a Philips TRx4841A and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2020· Philips North America, LLC

Recalled Item: TRx4851A 2.4 GHz IntelliVue Tele TRX Recalled by Philips North America, LLC...

The Issue: The ECG signal from patients being monitored using a Philips TRx4841A and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2020· Philips North America, LLC

Recalled Item: Phillips Azurion 7 M20 Recalled by Philips North America, LLC Due to No...

The Issue: No torque was specified for the four screws that connect the gearbox and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2020· Baxter Healthcare Corporation

Recalled Item: GEM Microvascular Anastomotic Coupler Devices - Product Usage: s intended...

The Issue: The Coupler size labeling of the outer tray may not match the Couper size...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2020· Baxter Healthcare Corporation

Recalled Item: GEM Microvascular Anastomotic Coupler Devices s intended to be used Recalled...

The Issue: The Coupler size labeling of the outer tray may not match the Couper size...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2020· Baxter Healthcare Corporation

Recalled Item: GEM Microvascular Anastomotic Coupler Devices - Product Usage: is intended...

The Issue: The Coupler size labeling of the outer tray may not match the Couper size...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2020· Respironics California, LLC

Recalled Item: Philips V60 Ventilators with Power Management PCBA part number 1055906...

The Issue: Solder connection failure on Power Management printed circuit board assembly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2020· Natus Neurology DBA Excel Tech., Ltd. (XLTEK)

Recalled Item: natus newborn care Olympic Brainz Monitor Recalled by Natus Neurology DBA...

The Issue: The OBM system functional test (impedance and noise) was not carried out on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2020· Skytron, Div. The KMW Group, Inc

Recalled Item: Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket Recalled...

The Issue: Potential for the weld to fail at the pivot point of the monitor bracket....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2020· Diagnostica Stago, Inc.

Recalled Item: STA - Deficient VIII Recalled by Diagnostica Stago, Inc. Due to A risk of...

The Issue: A risk of sample-to-sample cross-contamination of Emicizumab for factor VIII...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation standalone software treatment planning system Recalled by...

The Issue: Due to physical limitations of the treatment machine, the maximum field...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2020· Canon Medical System, USA, INC.

Recalled Item: Infinix-8000F with Catheterization Table CAT-850B or CAT-860B - Product...

The Issue: Bolts holding the longitudinal movement of catheterization tables may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2020· Canon Medical System, USA, INC.

Recalled Item: Infinix-8000V with Catheterization Table CAT-850B or CAT-860B - Product...

The Issue: Bolts holding the longitudinal movement of catheterization tables may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2020· Canon Medical System, USA, INC.

Recalled Item: Infinix-8000C with Catheterization Table CAT-850B or CAT-860B - Product...

The Issue: Bolts holding the longitudinal movement of catheterization tables may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2020· Capintec Inc

Recalled Item: Captus 4000e Thyroid Uptake System Recalled by Capintec Inc Due to It is...

The Issue: It is possible that the collimators have screw hole locations that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2020· Merits Holdings Co. dba Merits Health Products, Inc.

Recalled Item: Merits E604 Pilot Navigator Stairlift - Product Usage: To transport Recalled...

The Issue: Pinion gear may disengage from track allowing lift to slip or jolt.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2020· Argo Medical Technologies Ltd

Recalled Item: ReWalk Personal 6.0 Recalled by Argo Medical Technologies Ltd Due to ReWalk...

The Issue: ReWalk Robotics received two complaints (one in the US; one in the Germany),...

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

Class II — Potential Health HazardOngoing