Product Recalls in Kansas

Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,893 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,893 in last 12 months

Showing 1890118920 of 28,538 recalls

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

Recalled Item: Morris Lap Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

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: Universal Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

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: Facial Plastic Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

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: Lap Gallbladder Pack Recalled by Windstone Medical Packaging, Inc. Due to...

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: Lower Extremity Pack Recalled by Windstone Medical Packaging, Inc. Due to...

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: Bayview Abdominoplasty Pack Recalled by Windstone Medical Packaging, Inc....

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 Recon Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

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: Hernia Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

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: 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· 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 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 9, 2017· Aesculap Implant Systems LLC

Recalled Item: GN200 Caiman HF generators Recalled by Aesculap Implant Systems LLC Due to...

The Issue: Generators may have a faulty component which could impact the proper...

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

Class II — Potential Health HazardOngoing