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.
Showing 18341–18360 of 28,538 recalls
Recalled Item: 5.5mm Diameter x 500mm CoCr Straight Rod Recalled by XTANT MEDICAL INC Due...
The Issue: The material type on the label may incorrectly state Ti6Al-4V ELI . The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION PLUS¿ 8Fr. 50cc Intra-Aortic Balloon Catheter with Insertion Kit...
The Issue: Maquet/Getinge is initiating a voluntary product removal involving four lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amplia MRI Quad CRT-0 SureScan Claria MRI Quad CRT-D SureScan Recalled by...
The Issue: An unexpected transient mode switch behavior was detected by Medtronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OVATIO Models: VR 6250 Recalled by Sorin Group Italia SRL - CRF Due to Sorin...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PARADYM Models: VR 8250 Recalled by Sorin Group Italia SRL - CRF Due to...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTENSIA Models: VR 124 Recalled by Sorin Group Italia SRL - CRF Due to...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPoint¿ 500 Blood Gas Analyzer with v2.4 software for professional...
The Issue: Potential Patient Demographic Error with Blank Patient ID Field
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys PreciControl Varia 3 Recalled by Roche Diagnostics Corporation Due...
The Issue: e-barcode and value sheet for PreciControl Varia contains a typographical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CytoGuard Closed Luer Connector Recalled by B Braun Medical Inc Due to B....
The Issue: B. Braun is voluntarily recalling 13 lots of CytoGuard Closed Luer Connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit...
The Issue: The current secondary packaging, a box, incorrectly states that the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eMAG System Recalled by bioMerieux, Inc. Due to Some anomalies have been...
The Issue: Some anomalies have been identified during manufacturing controls.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fellows "Mighty 8" Power strip (Part Number 04175-0008) and TrippLite...
The Issue: Merge is conducting a hardware recall (replacement) of Fellows "Mighty 8"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 01.4mm x 457mm (18in) K-Wire Recalled by Amendia, Inc Due to Mislabeling
The Issue: Mislabeled guide wires - It was discovered that some Guide Wires labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for Recalled...
The Issue: Complaints concerning kinked haptics that were occurring during lens delivery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS CL Flow Cytometer Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter has confirmed that the Export feature located in the Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mederi Stretta Catheter and Accessory Kit Recalled by Mederi Therapeutics,...
The Issue: Product sterility compromised due to breach in sterile barrier package
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Second generation neoBLUE LED Phototherapy Light (neoBLUE 2) sold between...
The Issue: The second generation neoBLUE 2 lights with a black band, sold from 2003 to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATAR Reusable Extension Cable Recalled by Oscor, Inc. Due to The Reusable...
The Issue: The Reusable Oscor ATAR extension cables could separate from the connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi EndoWrist Suction Irrigator Recalled by Intuitive Surgical, Inc....
The Issue: Intuitive Surgical has become aware that in specific scenarios with system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATAR Disposable Extension Cable Recalled by Oscor, Inc. Due to The Reusable...
The Issue: The Reusable Oscor ATAR extension cables could separate from the connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.