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. 2,610 recalls have been distributed to Kansas in the last 12 months.
Showing 6101–6120 of 50,117 recalls
Recalled Item: IPS e.max ZirCAD CER/in. Prime B1 C17/5 -A zirconium oxide Recalled by...
The Issue: Defective blocks may show cracks after sintering If cracks are unnoticed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IPS e.max ZirCAD CER/in. Prime A1 C17/5 - A zirconium Recalled by IVOCLAR...
The Issue: Defective blocks may show cracks after sintering If cracks are unnoticed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliSpace Cardiovascular software Recalled by Philips Medical...
The Issue: Study data is not able to be archived, copied, or exported with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8000-021-002 Recalled by Stryker Leibinger GmbH & Co. KG Due to Unreleased...
The Issue: Unreleased software was installed on customer systems resulting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reagent Test Strips for Blood Recalled by Macherey Nagel Gmbh & Co. Kg Due...
The Issue: The reason for the recall is one of the test pads, for the parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InstaClear Lens Sheath. The InstaClear lens cleaner system and versatile...
The Issue: Potential for distal end of the sheath to break off during a procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Distal Access Catheter is a single-lumen Recalled by Stryker...
The Issue: Stryker Neurovascular is recalling their DAC- Distal Access Catheter -038...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyclophosphamide for Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...
The Issue: Labeling: Incorrect or missing Package Insert: There is an error on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyclophosphamide for Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...
The Issue: Labeling: Incorrect or missing Package Insert: There is an error on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Dako CoverStainer Recalled by Agilent Technologies Due to There...
The Issue: There is the potential for the front plexiglass door of the automated slide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile CoFlex NL: Latex Free Flexible Cohesive Bandage Recalled by Andover...
The Issue: A packaging seal gap could impact the sterility of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Airvo 2 Humidifier Recalled by Fisher & Paykel Healthcare, Ltd. Due to...
The Issue: Humidifier devices, used to deliver high flow respiratory therapy to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniLab Advanced + Ventilator Product Numbers 1111122 1111123 1111124...
The Issue: Device may experience an interruption or loss of therapy in case of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASER Application Instrument Recalled by Karl Storz Endoscopy Due to Laser...
The Issue: Laser surgical instruments have no specific evidence of a validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eyesaline Recalled by HONEYWELL INC Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A...
The Issue: Due to unsupported 10 year expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOSPA Patella Component Model/Catalog Number: 01.10.9XX Software Version:...
The Issue: Due to unsupported 10 year expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Oncology Essentials Package of the Spectral CT imaging system. Recalled...
The Issue: Potential for third party oncology marking laser to be off the gantry cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 1 Recalled by Stryker Leibinger GmbH & Co. KG Due to Mislabeling
The Issue: Mislabeled: Product labeled 56-90614 (90x90 Gold Mesh), was actually...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atovaquone Oral Suspension USP Recalled by AvKARE Due to Microbial...
The Issue: Microbial contamination of a non-sterile product: potential Bacillus cereus...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.