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 2762127640 of 29,505 recalls

Medical DeviceMarch 1, 2013· American Medical Systems, Inc.

Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...

The Issue: American Medical Systems, Inc. is initiating a recall on two components of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: Roche Molecular Systems cobas x 480 System 50 mL reagent reservoir Recalled...

The Issue: Certain lots of Reagent reservoirs, may not have a separation in the lower...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2013· B. Braun Medical, Inc.

Recalled Item: Diacap(R) Ultra Dialysis Fluid Filter Recalled by B. Braun Medical, Inc. Due...

The Issue: There is the potential of the residual moisture of the Diacap Ultra membrane...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2013· Allen Medical Systems, Inc.

Recalled Item: Allen Traction Boot Recalled by Allen Medical Systems, Inc. Due to Some...

The Issue: Some units may have been assembled incorrectly which could result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Mammomat Inspiration - full-field digital mammography Product Usage:...

The Issue: Firm became aware of an unintended behavior when using the Mammomat...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2013· Vascular Solutions, Inc.

Recalled Item: Vascular Solutions Recalled by Vascular Solutions, Inc. Due to Risk that air...

The Issue: Risk that air may be introduced into the device which may lead to an air...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 27, 2013· Sirtex Medical Limited

Recalled Item: Sirtex SIR-yttrium 90 microspheres (Radionuclide) Recalled by Sirtex Medical...

The Issue: Incorrect expiration date

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

Class III — Low RiskOngoing
Medical DeviceFebruary 27, 2013· Natus Neurology Incorporated

Recalled Item: Nicolet EEG Wireless Amplifier 32/64 Channel. Catalog/Part Numbers :...

The Issue: Natus Neurology Incorporated is recalling the Nicolet EEG Wireless Amplifier...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial and Venous Recalled...

The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic Prostiva RF Therapy Generator. The Prostiva RF system is Recalled...

The Issue: Medtronic has found through device testing that if the optional footswitch...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial and Venous Recalled...

The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI Blood Parameter Monitoring System 500 with Venous blood parameter...

The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...

The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...

The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2013· Hospira Inc.

Recalled Item: The LifeCare PCA infusion system with Hospira MedNet software allows...

The Issue: The infusion pump has a clear plastic door that, due to its design, allows...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2013· Hospira Inc.

Recalled Item: The PCA 3 infusion pump allows clinicians Recalled by Hospira Inc. Due to...

The Issue: The infusion pump has a clear plastic door that, due to its design, allows...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2013· Neurotherm, Inc.

Recalled Item: Neurotherm Curved Radiofrequency (RF) cannnula 10 cm 18 gauge Recalled by...

The Issue: Straight needle labeled as a curved needle

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Cube Pessary w/Drainage Holes #0"1" Recalled by Cooper...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Hill-Rom, Inc.

Recalled Item: TotalCare SpO2RT2 bed. Product Usage: Bed Recalled by Hill-Rom, Inc. Due to...

The Issue: In certain situations a software problem with the TotalCare SpO2RT¿ 2 bed...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Incontinence Dish w/ Support Pessary #0 Recalled by Cooper...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing