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. 1,059 recalls have been distributed to Kansas in the last 12 months.
Showing 15701–15720 of 50,117 recalls
Recalled Item: Kit: Injection REVIEW MAI Kit Part Number: 74736 Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FISTULA (ON/OFF) ALL IN ONE BAG. Medical convenience kit Recalled by Avid...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angio Pack Recalled by Windstone Medical Packaging, Inc. Due to Angio tubing...
The Issue: Angio tubing included within Custom Convenience kits may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angio Pack Recalled by Windstone Medical Packaging, Inc. Due to Angio tubing...
The Issue: Angio tubing included within Custom Convenience kits may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene SARS-CoV-2 Catalog Number: 410700 IVD for real-time Reverse...
The Issue: Emergency Use Application (EUA) application withdrawn as false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene RNA Software Upgrade Kit Revogene RNA Software Upgrade USBs...
The Issue: Emergency Use Application (EUA) application withdrawn as false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CANNU-Flex SILK Interference Screws 6 mmx 30 mm - Product Recalled by Smith...
The Issue: Mislabeled box contained a 6mm x 20mm screw instead of 6mm x 30mm screw
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premium OrgaZEN 7000 capsule Recalled by NSNY Distributor Inc Due to...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ginseng Power 5000 capsule Recalled by NSNY Distributor Inc Due to...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt HF Quad MRI SureScan Implantable Cardioverter Defibrillators with...
The Issue: The device may contain a manufacturing defect of a missing resistance spot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.