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. 2,598 recalls have been distributed to Kansas in the last 12 months.
Showing 8481–8500 of 28,538 recalls
Recalled Item: BioPlex 2200 SYPH T PACK Syphilis Total & RPR Reagent Pack Recalled by...
The Issue: Due to current concerns related to COVID-19 vaccine interference with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Syphilis Total & RPR Calibrator Set CAL Recalled by Bio-Rad...
The Issue: Due to current concerns related to COVID-19 vaccine interference with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The IFU for the Autoclavable Temperature Probes: Part # 453564635891...
The Issue: Update to instructions for use regarding the cleaning and disinfection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brius Patient Specific Brackets (components in a set of custom Recalled by...
The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Customized Brius Appliances (custom metal orthodontic devices) Recalled by...
The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brius Pontics (components in a set of custom metal orthodontic devices)...
The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to There is a potential...
The Issue: There is a potential for AED pads to experience gel separation from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to There is a potential...
The Issue: There is a potential for AED pads to experience gel separation from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic TurboHawk Plus Directional Atherectomy System 6F Recalled by ev3...
The Issue: The device has similarities in design to another device that the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic TurboHawk Plus Directional Atherectomy System 6F Recalled by ev3...
The Issue: The device has similarities in design to another device that the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiovascular Procedure Kit catalog # 76645 & 73806 Recalled by Terumo...
The Issue: Potential for Cardiovascular Procedure Kit packaging damage that occurred...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MM-TSM (Touch Screen Module/Secondary Controller/Bedside Controller)...
The Issue: Multi-Modality Touch Screen Modules (MM-TSM), used with integrated IVUS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity s System software version2.8.0 Recalled by Abbott Laboratories, Inc...
The Issue: Software error associated with the immunoassay analyzer wash cycle which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips StentBoost Live R2.0 application Recalled by Philips Healthcare Due...
The Issue: Due to an incorrect configuration setting in the EPX database of StentBoost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura (Model Numbers 722010 Recalled by Philips North America Llc...
The Issue: Due to a software defect, the Philips StentBoost Live R2.0 might not process...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NuOss Collagen Block Size 8mm x 9mm x 9mm- used Recalled by Ace Surgical...
The Issue: NuOss Collagen (dental) was packaged with a Collatene Fibrillar Collagen(for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) JOBST Compri2 Recalled by BSN Medical Inc Due to Mislabeling
The Issue: The folding boxes within the shipping case are mislabeled. The shipping case...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mevion S250 and S250i Proton Therapy Systems hand pendant (P/N Recalled by...
The Issue: Malfunction of the hand pendant controlling movement of the therapy couch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L Recalled by BioPro,...
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MD Recalled by BioPro,...
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.