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. 1,893 recalls have been distributed to Kansas in the last 12 months.
Showing 19841–19860 of 28,538 recalls
Recalled Item: NOMAD Pro2 Packaged X-Ray System Recalled by Aribex Inc Due to Firm received...
The Issue: Firm received customer complaints where end users reported that Nomad Pro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FrameLink. The software application is sent in CD format with an IFU...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVX-450NR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...
The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD) Recalled by Becton, Dickinson...
The Issue: Internal review found that some vials of CD3/CD4/CD45 state that the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MACH Cranial Treon. The software application is sent in CD format with an...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S7 MACH FrameLink. The software application is sent in CD format with an IFU...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVX-330NR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...
The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MACH AxiEM Cranial Treon. The software application is sent in Recalled by...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVX-330BR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...
The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fusion ENT Application. The software application is sent in CD Recalled by...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RSD 800 Sorting System calculator/data processing module Recalled by Roche...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affinity Four Birthing Bed Model P3700 The primary packaging is Recalled by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS II Aliquoter System calculator/data processing module Recalled by Roche...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System Recalled by Elekta, Inc. Due to It is...
The Issue: It is possible that a change to an Order Set will not be saved in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Articulating Linear Cutter Recalled by Ethicon Endo-Surgery Inc...
The Issue: Quality control identified a component issue where the pinion gear in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Pre Analytics ( EVO/Plus) Product Usage: The RSD 800A Recalled by...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche COBAS INTEGRA 800 /800 CTS Analyzer Analyzer Recalled by Roche...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas 6000 Series system c6000 Recalled by Roche Diagnostics Operations,...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e411 Immunoassay Analyzer e411: Immunoassay Analyzer Product Usage:...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas 6800/8800 system Hepatitis Viral B DNA Detection Product Usage:...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.