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. 2,348 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,348 in last 12 months

Showing 4190141920 of 50,117 recalls

Medical DeviceJuly 9, 2014· Carestream Health, Inc.

Recalled Item: Kodak DirectView DR 7500 Diagnostic X-Ray System Product Usage: The Recalled...

The Issue: An on-site evaluation of the equipment parts that attach the Beta Assembly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2014· Teleflex Medical

Recalled Item: Hudson RCI Recalled by Teleflex Medical Due to The temperature probe does...

The Issue: The temperature probe does not properly connect to the temperature port.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2014· Teleflex Medical

Recalled Item: Hudson RCI Recalled by Teleflex Medical Due to The temperature probe does...

The Issue: The temperature probe does not properly connect to the temperature port.

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

Class II — Potential Health HazardOngoing
DrugJuly 8, 2014· Pfizer Inc.

Recalled Item: VIRACEPT (R) (nelfinavir mesylate) Tablets Recalled by Pfizer Inc. Due to...

The Issue: Labeling: Incorrect or missing lot and or Exp Date: The bottles were labeled...

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

Class III — Low RiskOngoing
Refund
FoodJuly 8, 2014· Michael Foods, Inc.

Recalled Item: Shell Eggs packaged under the following labels: (1) Abbotsford Farms...

The Issue: Shell eggs contaminated with Pseudomonas fluorescens.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodJuly 8, 2014· Seoul Shik Poom, Inc.

Recalled Item: Choripdong Chocolate Almond Richmond Ice Bar 4 bars/432 mL Seoul Recalled by...

The Issue: Seoul Trading USA Inc. is recalling Choripdong Chocolate Almond Richmond Ice...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 8, 2014· Gyrus Medical, Inc

Recalled Item: Gyrus ACMI Falope-Ring Dilator Recalled by Gyrus Medical, Inc Due to...

The Issue: Falope-Ring Dilator for Reusable Falope-Ring Band Applicators have been sold...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Stryker Spine

Recalled Item: Specialty Aria Inserter Recalled by Stryker Spine Due to Stryker has...

The Issue: Stryker has initiated the recall of its Aria Standard and Specialty Implant...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Luminos dRF Recalled by Siemens Medical Solutions USA, Inc Due to It...

The Issue: It was discovered that during a RAD examination using Siemens Luminos dRF,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Stryker Spine

Recalled Item: Stryker Aria Implant Inserter Recalled by Stryker Spine Due to Stryker has...

The Issue: Stryker has initiated the recall of its Aria Standard and Specialty Implant...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Possible sound loss...

The Issue: Possible sound loss associated with the CARESCAPE Monitor B650. When an...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4051 Endo Tube Holder Recalled by Smiths Medical ASD, Inc. Due to The tube...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4002S Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4052 Endo Tube Holder Recalled by Smiths Medical ASD, Inc. Due to The tube...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4002PS Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: 4001PS Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4001S Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...

The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System --- For use in the in vitro quantitative...

The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System --- For use in the in vitro quantitative...

The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...

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

Class II — Potential Health HazardOngoing