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. 2,636 recalls have been distributed to Kansas in the last 12 months.
Showing 1561–1580 of 28,538 recalls
Recalled Item: Medline convenience kits containing BD Insyte Autoguard Shielded IV...
The Issue: Medline Industries, LP. is issuing a recall for specific Medline kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroMyst Applicator Recalled by Integra LifeSciences Corp. (NeuroSciences)...
The Issue: Lack of sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIONE Model 30-0001 UDI-DI code: 03760305400031 The EPIONE¿ device is...
The Issue: Due to a software bug the robotic arm may incorrectly guide the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IontoPatch 80 Recalled by LTS Therapy Systems, LLC Due to The nonwoven pads...
The Issue: The nonwoven pads in the device do not absorb the saline solution or any...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IontoPatch STAT Recalled by LTS Therapy Systems, LLC Due to The nonwoven...
The Issue: The nonwoven pads in the device do not absorb the saline solution or any...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Cardiology Hemodynamics Software Recalled by CHANGE...
The Issue: Due to complaints, software update may cause software to unexpectedly shutdown.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Cardiology Hemo Software Recalled by CHANGE HEALTHCARE...
The Issue: Due to complaints, software update may cause software to unexpectedly shutdown.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extended Tip Applicator Recalled by Integra LifeSciences Corp....
The Issue: Devices contain potentially out-of-specification levels of endotoxins and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extended Tip Applicator Recalled by Integra LifeSciences Corp....
The Issue: Devices contain potentially out-of-specification levels of endotoxins and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jewel Precision Reusable Rigid Sterilization Container System. Model/Catalog...
The Issue: The Instructions for Use do not match the 510(k) FDA cleared indications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product: Atellica CH Diluent - CONS 2 x 1.5L Recalled by Siemens Healthcare...
The Issue: Contamination of the diluent by sodium hypochlorite (NaOCl) which may impact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extended Tip Applicator 8CM Recalled by Integra LifeSciences Corp....
The Issue: Devices contain potentially out-of-specification levels of endotoxins and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to Investigation determined that...
The Issue: Investigation determined that one lot of the T2 Greater Trochanter Nail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to Investigation determined that...
The Issue: Investigation determined that one lot of the T2 Greater Trochanter Nail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insyte Autoguard Shielded IV Catheter Recalled by Becton Dickinson...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insyte Autoguard Winged Shielded IV Catheter Recalled by Becton Dickinson...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insyte Autoguard Shielded IV Catheter Recalled by Becton Dickinson...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.