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 1501–1520 of 28,538 recalls
Recalled Item: Azurion 7 M20. Fluoroscopic X-Ray System. Recalled by PHILIPS MEDICAL...
The Issue: Potential for bolts connecting the gearbox to the mounting flange of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: T4 Total ELISA Product Name: T4 Total ELISA Recalled by DRG...
The Issue: An incoming complaint reported that the expiration date on the kit box label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zvu Anorectal Manometry Procedure Kit Recalled by Diversatek Healthcare Due...
The Issue: Anorectal manometry procedure kit outer kit label is mislabeled with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN1 Control) Recalled by...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN2 Control) Recalled by...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve Recalled by...
The Issue: Due to a manufacturing issue, disinfecting cap for needle-free connectors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by C.R. Bard Inc Due to Cather packaging may contain the incorrect...
The Issue: Cather packaging may contain the incorrect French size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bravo CF capsule delivery device Recalled by Given Imaging Ltd. Due to It...
The Issue: It has been determined that misapplied adhesive on the Bravo CF capsule...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton C6 (ESM Board PN 10144626 UDI-DI code: Recalled by Hamilton Medical...
The Issue: A mechanical defect on a printed circuit board (PCB) as a result of PCB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Heyman Follower Coude Tip for following sizes: 12Fr - Recalled by C.R....
The Issue: Cather packaging may contain the incorrect French size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Heyman Follower Straight Tip for following sizes: 10Fr - Recalled by C.R....
The Issue: Cather packaging may contain the incorrect French size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medshape Universal Joints Recalled by Medshape, INC. Due to Bone external...
The Issue: Bone external fixation system may have the pin that can become dislodged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-u Ventilator System. Model Number: 6688600. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inseego USB8 4G Dongle Kit Recalled by Remote Diagnostic Technologies Ltd....
The Issue: Kit USB flash drive contains outdated software, which could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platelia Toxo IgM Catalog Number 26211 UDI Code: 03610520005552 The Recalled...
The Issue: Due to a risk of false positive results that could lead to unnecessary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-n Ventilator System. Model Number: 6694800. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-u MR Ventilator System. Model Number: 6888800. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva Nova-Dual Product Number: 781173 Recalled by Philips...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Explorer/Nova Dual Product Number: 781108 Recalled by Philips...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T¿ Recalled by Philips North America Due to...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.