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. 1,019 recalls have been distributed to Kansas in the last 12 months.
Showing 21101–21120 of 50,117 recalls
Recalled Item: Endotrac EPF/EGR Push Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Urinalysis Control Level 2 (IVD) - Product Recalled by Randox...
The Issue: Analyte range for Leukocytes for use with the Siemens Multistix method is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Hook Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrig ETF Hook Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.CT software version VA48A_SP5.5 in the following SOMATOM computed...
The Issue: SOMATOM Definition Edge, SOMATOM Definition AS, SOMATOM Definition Flash...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WS80A Diagnostic Ultrasound System Version 1.00.16 Recalled by NeuroLogica...
The Issue: There is a potential for probes overheating when decreasing the Doppler SV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Triangle Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Hook Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Hook Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 133 Tissue Expanders w/Suture Tabs BIOCELL Full Height Variable...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 133 Tissue Expanders (also named style 133 BIOSPAN Tissue Recalled...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc. Due to...
The Issue: Potential for Hemospray device to be unable to spray powder due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle and McGhan 410 TruForm 2 (Soft Touch) BIOCELL breast implant...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 410 Recalled by Allergan PLC Due to The action was initiated...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RITZ PRINCESS Recalled by Allergan PLC Due to The action was initiated...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle Inspira Recalled by Allergan PLC Due to The action was initiated...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle and McGhan Silicone-Filled Breast Implants Recalled by Allergan PLC...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle and McGhan Silicone-Filled Breast Implant BioCell Round Moderate...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 510 Recalled by Allergan PLC Due to The action was initiated...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle Recalled by Allergan PLC Due to The action was initiated following...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.