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 2510125120 of 29,201 recalls

Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: LAP AROSCOPY PACK - (10) GAUZE SPONGE 4" X 4" Recalled by Customed, Inc Due...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: Obstetrical Surgical pack Recalled by Customed, Inc Due to Customed has...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: CYSTO TUR PACK- - (1) UTILITY BOWL 32oz LIF (1) Recalled by Customed, Inc...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: AV FISTULA PACK- (1) DRAPE T LAPAROT 102" X 78" Recalled by Customed, Inc...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: Open Heart Tray Recalled by Customed, Inc Due to Customed has determined...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: PERl GYN PACK- (1) DRAPE UTILITY WITH TAPE UF (2) Recalled by Customed, Inc...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: LAPAROSCOPY COLORECTAL SURGICAL PACK CONTENTS: (1) SOLUTION SURGICAL...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: ANGIOGRAPHY PACK- - (4) CLOTH HUCK TOWEL BLUE UF (1) Recalled by Customed,...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: HIP PACK I (2) Recalled by Customed, Inc Due to Customed has determined that...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: GENERAL MINOR PACK- (1) MAYO STAND COVER REINFORCED LIF (2) Recalled by...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· SCC Soft Computer

Recalled Item: SoftLab with SA HIS versions 4.0.7.0-4.0.7.1 SoftLab is a laboratory...

The Issue: The interface fails to send abnormal flags for Lab test results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: syngo Lab Data Manager Recalled by Siemens Healthcare Diagnostics, Inc. Due...

The Issue: Certain configuration parameters may cause the ranges to not hold results as...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· KCI USA, Inc.

Recalled Item: CelluTome Epidermal Harvesting System Part number CT-H25 or Part Number...

The Issue: Blade can shift during shipping which makes the product ineffective.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Small Bone Innovations

Recalled Item: Small Bone Innovations 3.0/4.0mm AutoFIX" Cannulated Compression Screw...

The Issue: Small Bone Innovations (SBi) is recalling all lots of 3.0/4.0mm AutoFIX"...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing