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 2664126660 of 29,201 recalls

Medical DeviceJune 17, 2013· CareFusion 303, Inc.

Recalled Item: Alaris PC unit Recalled by CareFusion 303, Inc. Due to CareFusion is...

The Issue: CareFusion is recalling the Alaris PC units model 8015 (PC unit), version...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: The SurgiCounter Charging Cradle Product Usage: SurgiCounter Charging...

The Issue: Faulty SurgiCounter Charging Cradle can prevent the scanner from charging or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· PIONEER SURGICAL TECHNOLOGY, INC.

Recalled Item: Streamline MIS Spinal Fixation System Fixed Rod Holder NON STERILE Recalled...

The Issue: The affected fixed rod holders did not allow the instrument to lock down on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2013· GE Healthcare, LLC

Recalled Item: Discovery NM 630 Recalled by GE Healthcare, LLC Due to GE became aware of an...

The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 13, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Varicam/VG and VG Hawkeye devices Product Usage: The Recalled...

The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...

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

Class I — Serious Health HazardOngoing