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. 2,423 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,423 in last 12 months

Showing 2602126040 of 50,117 recalls

Medical DeviceMay 14, 2018· Opgen Inc

Recalled Item: AdvanDx QuickFISH Slides Recalled by Opgen Inc Due to Possible diminished...

The Issue: Possible diminished performance prior to its established expiration date.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2018· Beaver Visitec

Recalled Item: Safety Sideport Knife 1.0mm 45¿ Recalled by Beaver Visitec Due to Blades are...

The Issue: Blades are loose in handles and may fall out due to non cured epoxy

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2018· Merck Millipore Ltd.

Recalled Item: Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031...

The Issue: In vitro diagnostic devices, used greater than 6 months after date of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus JF-140F duodenoscopes (Model NumberJF-140F) Recalled by Olympus...

The Issue: Issuance of validated, new reprocessing procedures. This corrective action...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2018· Zimmer Biomet, Inc.

Recalled Item: Vanguard Knee System PS Tibial Bearing Recalled by Zimmer Biomet, Inc. Due...

The Issue: The label master file was errantly set up as a 63/37mm instead of a 63/67mm....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus JF-160F duodenoscopes (Model NumberJF-160F) Recalled by Olympus...

The Issue: Issuance of validated, new reprocessing procedures. The new cleaning...

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

Class II — Potential Health HazardOngoing
DrugMay 11, 2018· L. Perrigo Company

Recalled Item: Scopolamine Transdermal Therapeutic System Recalled by L. Perrigo Company...

The Issue: Defective delivery system

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Drive System Recalled by FHC, Inc. Due to The FHC Depth Stop...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Mako Surgical Corporation

Recalled Item: Rio System Irrigation Clip - Catalog # 111690 Product Usage: Recalled by...

The Issue: Out of tolerance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Microintroducer Kit Recalled by Angiodynamics Inc. (Navilyst Medical Inc.)...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: RS 5F DL BIOFLO PASV Recalled by Angiodynamics Inc. (Navilyst Medical Inc.)...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: RS TANDEM 5F DL BIOFLO PICC Recalled by Angiodynamics Inc. (Navilyst Medical...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BioFlo PICC (NV) 5FDL-55cm Maximal Barrier Nursing Kit w/70cm Nitinol Wire...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved with Nitinol Guidewire PG...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: RS 5F DL XPP Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due to A...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BioFlo PICC (Valved) 5FDL-55cm Maximal Barrier Nursing Kit w/70cm Nitinol...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: RS TANDEM 5F DL BIOFLO PASV Recalled by Angiodynamics Inc. (Navilyst Medical...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F SL-55CM IR-145 Kit Non-Valved with Nitinol GW PG Recalled by...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: TANDEM 5F DL BIOFLO PASV Recalled by Angiodynamics Inc. (Navilyst Medical...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BioFlo PICC (Valved) 5FDL-55cm Maximal Barrier Nursing Kit PG Recalled by...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing