Product Recalls in Louisiana

Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,506 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,506 in last 12 months

Showing 2850128520 of 29,201 recalls

Medical DeviceJune 12, 2012· Maquet Cardiovascular Us Sales, Llc

Recalled Item: QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator Recalled by Maquet...

The Issue: It has come to firm's attention that, in some rare cases, the blood outlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...

The Issue: GE Healthcare has become aware through complaints of a potential safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2012· Teleflex Medical

Recalled Item: Hudson RCI Concha Therm Neptune Humidifier Recalled by Teleflex Medical Due...

The Issue: Speaker Failure. If the speaker fails and an event occurs which would...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2012· Tedan Surgical Innovations Llc

Recalled Item: Sterile Distraction Screws of 3 different sizes: 12mm Recalled by Tedan...

The Issue: This letter is to notify you that several of our sterile screw products are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a Image Flip Issue associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a Image Flip Issue associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Neptune 1 Gold Rover (120 Vand 230V ) Waste Management Recalled by Stryker...

The Issue: Stryker has received two reports of serious injury as a result of tissue...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Neptune Bronze Rover Recalled by Stryker Instruments Div. of Stryker...

The Issue: Stryker has received two reports of serious injury as a result of tissue...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a Image Flip Issue associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2012· Merit Medical Systems, Inc.

Recalled Item: Custom Procedural Trays: Merit's Custom Total Hip Pack Recalled by Merit...

The Issue: Custom Procedural trays contain Stryker Hytrel Togas which are being...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Neptune 1 Silver Rover Recalled by Stryker Instruments Div. of Stryker...

The Issue: Stryker has received two reports of serious injury as a result of tissue...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2012· Philips And Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 16 Multi-Slice CT Scanner System is a computed Tomography X-ray...

The Issue: One of the four screws that secure the Oil-accumulator to the X-Ray Tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Neptune Rover Waste Management System Recalled by Stryker Instruments Div....

The Issue: Stryker has received two reports of serious injury as a result of tissue...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 7, 2012· Arrow International Inc

Recalled Item: Arrow International Recalled by Arrow International Inc Due to Arrow is...

The Issue: Arrow is recalling the product due to the possibility of voids in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: EasyLink(TM) Informatics System Recalled by Siemens Healthcare Diagnostics,...

The Issue: There is a potential for the EasyLink system to display and transmit to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens syngo(R) Lab Data Manager. The syngo(R) Lab Data Manager Recalled by...

The Issue: The recalling firm has discovered that when using a Sysmex(R) CA-7000 or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2012· Integra LifeSciences Corp. d.b.a. Integra Pain Management

Recalled Item: Single Shot Epidural Trays Recalled by Integra LifeSciences Corp. d.b.a....

The Issue: Integra LifeSciences is recalling one lot of Single Shot Epidural Trays as...

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

Class III — Low RiskOngoing
Medical DeviceJune 7, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Stratus(R) CS Acute Care(TM) D-dimer Calibrator (DDM CalPak) lots...

The Issue: Siemens has confirmed that the Stratus(R) CS Acute Care(TM) D-Dimer CalPak...

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

Class III — Low RiskOngoing
Medical DeviceJune 6, 2012· Zoe Medical Incorporated

Recalled Item: Spacelabs Ultraview DM3 Monitor Model Number: 91330-NT The Ultraview DM3...

The Issue: Unit fails to power up, resulting in an equipment alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens syngo.plaza radiological image processing system. Recalled by...

The Issue: Siemens became aware of an unintended behavior when using syngo.plaza. In...

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

Class II — Potential Health HazardOngoing