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. 1,090 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,090 in last 12 months

Showing 6861–6880 of 28,538 recalls

Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Insulin Syringes with the BD Micro-Fine IV Needle 0.5ml Recalled by...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Ultra-Fine Insulin Syringe 0.5mL Recalled by Becton Dickinson & Company...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Synthes (USA) Products LLC

Recalled Item: TFN-Advanced Femoral Nail 12MM/125 DEG TI CANN TFNA 200MM STERILE. Recalled...

The Issue: TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: Power-PRO 2 . Intended as an ambulance cot to transport Recalled by Stryker...

The Issue: Transport Cot has insufficient volume of epoxy to assemblies installed in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Preat Corp

Recalled Item: PREAT NOBIL GRIP Recalled by Preat Corp Due to Product is labeled with an...

The Issue: Product is labeled with an incorrect expiration date.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Ultra-Fine II Insulin Syringe 0.5mL Recalled by Becton Dickinson &...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Synthes (USA) Products LLC

Recalled Item: TFN-Advanced Femoral Nail 12MM/125 DEG TI CANN TFNA 170MM - Recalled by...

The Issue: TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Scientia Vascular, Inc.

Recalled Item: Plato 17 Microcatheter: Straight Tip Recalled by Scientia Vascular, Inc. Due...

The Issue: Microcatheters for embolic coil and diagnostic agent introduction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Ultra-Fine Insulin Syringe 1mL Recalled by Becton Dickinson & Company Due...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Synthes (USA) Products LLC

Recalled Item: TFN-Advanced Femoral Nail 12MM/130 DEG TI CANN TFNA 170MM STERILE. Recalled...

The Issue: TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· Carestream Health, Inc.

Recalled Item: DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For...

The Issue: After pressing and releasing the Z-Axis Motorized buttons on the Tube Head...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· Maquet Cardiovascular, LLC

Recalled Item: Fusion Bioline Vascular Graft Recalled by Maquet Cardiovascular, LLC Due to...

The Issue: One (1) Fusion Bioline Vascular graft from lot 25162546, which failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· DiaSorin Molecular LLC

Recalled Item: Simplexa COVID-19 Direct Recalled by DiaSorin Molecular LLC Due to Direct...

The Issue: Direct amplification Discs , used with COVID-19 and Flu A/B & RSV assays,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Tacrolimus (TAC) Flex reagent cartridge-In vitro diagnostic test...

The Issue: Siemens Healthineers has received customer complaints and confirmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· DiaSorin Molecular LLC

Recalled Item: Simplexa Flu A/B & RSV Direct Gen II Recalled by DiaSorin Molecular LLC Due...

The Issue: Direct amplification Discs , used with COVID-19 and Flu A/B & RSV assays,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· Carefusion 2200 Inc

Recalled Item: CD5 Series of Genesis Reusable Rigid Sterilization Container Systems catalog...

The Issue: Product did not meet shelf-life testing requirements resulting in a breach...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH LDL Cholesterol Direct (DLDL)-In vitro diagnostic quantitative...

The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Total Protein II- In vitro diagnostic use in Recalled by Siemens...

The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Triglycerides_2: in vitro diagnostic use in the quantitative...

The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Triglycerides (concentrated)-In vitro diagnostic use in the...

The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...

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

Class II — Potential Health HazardOngoing