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. 2,398 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,398 in last 12 months

Showing 3608136100 of 50,117 recalls

Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: INTEGRIS BV3000 MONO Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD20 OR Table Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD20/15 Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD20/20 Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: UNIQ FD OR table Recalled by Philips Electronics North America Corporation...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· St Jude Medical Cardiac Rhythm Management Division

Recalled Item: Optisure Dual Coil Defibrillation Leads Recalled by St Jude Medical Cardiac...

The Issue: Leads may have been compromised during the manufacturing process, with cuts...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 3, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...

The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 3600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA CLINIC PATCH 3.2.0 CD Product Usage: MYLA is a Recalled by bioMerieux,...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA MASTER DVD 3.2 CLI DL380 Product Usage: MYLA is Recalled by bioMerieux,...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA CLI V3.X TO V4.1 ML350 SERVER Product Usage: MYLA Recalled by...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA CLI V3.X TO V4.1 DL380 SERVER Product Usage: MYLA Recalled by...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA CLINIC PATCH 3.3.0 CD Product Usage: MYLA is a Recalled by bioMerieux,...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA MASTER DVD V4.1 CLI Product Usage: MYLA is a Recalled by bioMerieux,...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA MASTER DVD V4.0 CLI Product Usage: MYLA is a Recalled by bioMerieux,...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
DrugNovember 2, 2015· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Meclizine Hydrochloride Tablets Recalled by Mylan Institutional, Inc....

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 2, 2015· Trumpf Medical Systems, Inc.

Recalled Item: Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted...

The Issue: The firm has received 15 complaints over ten years related to the connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2015· Insulet Corporation

Recalled Item: OmniPod¿ Recalled by Insulet Corporation Due to Pod's needle mechanism fails...

The Issue: Pod's needle mechanism fails to deploy or there is a delay in the deployment...

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

Class I — Serious Health HazardOngoing