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. 2,547 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,547 in last 12 months

Showing 1924119260 of 29,201 recalls

Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Stem Pack Recalled by Windstone Medical Packaging, Inc. Due to The Medtronic...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Breast Augmentation Pack Recalled by Windstone Medical Packaging, Inc. Due...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Arrow International Inc

Recalled Item: Vascular catheter introduction kit The PICC is indicated for short Recalled...

The Issue: There have been complaints for peel away sheaths flaring

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: N Latex HCY REAGENT Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: The firm confirmed a reduced once-opened and on-board stability for N Latex...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Mammomat Inspiration full Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Software error

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Ortho Kinematics, Inc

Recalled Item: Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a Recalled...

The Issue: Ortho Kinematics Inc. sent a Notice of Correction to Released Testing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2017· Elekta, Inc.

Recalled Item: Monaco RTP System. Used to make treatment plans for patients Recalled by...

The Issue: Incorrect dose after editing beam number an wedge angle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2017· Encore Medical, Lp

Recalled Item: LIMA Modular Revision Hip Stem Model 428-01-050_110 Product Usage: The...

The Issue: Lima Proximal Bodies were inadvertently re-sterilized. The safety screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2017· Encore Medical, Lp

Recalled Item: Empowr PS Knee Tibial Insert Recalled by Encore Medical, Lp Due to The...

The Issue: The Empowr PS Insert was reported as missing the impaction slot feature.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2017· Resource Optimization & Innovation Llc

Recalled Item: Regard Recalled by Resource Optimization & Innovation Llc Due to Custom...

The Issue: Custom procedure trays contain a component, a light glove, that has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2017· Resource Optimization & Innovation Llc

Recalled Item: Regard Recalled by Resource Optimization & Innovation Llc Due to Custom...

The Issue: Custom procedure trays contain a component, a light glove, that has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2017· Resource Optimization & Innovation Llc

Recalled Item: Regard Recalled by Resource Optimization & Innovation Llc Due to Custom...

The Issue: Custom procedure trays contain a component, a light glove, that has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2017· Resource Optimization & Innovation Llc

Recalled Item: Regard Recalled by Resource Optimization & Innovation Llc Due to Custom...

The Issue: Custom procedure trays contain a component, a light glove, that has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2017· Resource Optimization & Innovation Llc

Recalled Item: Regard Recalled by Resource Optimization & Innovation Llc Due to Custom...

The Issue: Custom procedure trays contain a component, a light glove, that has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2017· Resource Optimization & Innovation Llc

Recalled Item: Regard Recalled by Resource Optimization & Innovation Llc Due to Custom...

The Issue: Custom procedure trays contain a component, a light glove, that has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2017· Resource Optimization & Innovation Llc

Recalled Item: Regard Recalled by Resource Optimization & Innovation Llc Due to Custom...

The Issue: Custom procedure trays contain a component, a light glove, that has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2017· Resource Optimization & Innovation Llc

Recalled Item: Regard Recalled by Resource Optimization & Innovation Llc Due to Custom...

The Issue: Custom procedure trays contain a component, a light glove, that has been...

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

Class II — Potential Health HazardOngoing