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. 1,854 recalls have been distributed to Kansas in the last 12 months.
Showing 24921–24940 of 28,538 recalls
Recalled Item: Synthes 5.0mm Variable Locking Screw This device is part of Recalled by...
The Issue: Labeling correction: The package insert in one 5.0mm Variable Locking Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fisherbrand Sterile Swabs Recalled by Fisher Scientific Co Due to A customer...
The Issue: A customer reported the presence of an organism in a lot of Calcium Alginate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Brand Name(s): Alere Triage¿ TOX+MTD Drug Screen Recalled by Alere...
The Issue: Alere San Diego, Inc. is initiating a recall of the Alere Triage¿ TOX Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Flu AlB & RSV Direct Assay Kits Recalled by Focus Diagnostics Inc...
The Issue: Focus Diagnostics initiated the recall of the certain Simplexa Flu AlB & RSV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F180NRe High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F200A High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F180NR High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F200NR High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F160NR High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F18Nre Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux B200 Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F200NRe High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator used Model numbers: M3535A...
The Issue: HeartStart MRx Defibrillator Monitor therapy connection could experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F160NRe High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amo-O Herbal Stimulator Recalled by Altasource LLC dba Meta Labs LLC Due to...
The Issue: Firm is not registered as a drug manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Recalled by Siemens Medical Solutions Diagnostics Due to There...
The Issue: There is a potential for incorrect results to be reported from processing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Citation TMZF HA 132 degrees Neck Angle Recalled by Stryker Howmedica...
The Issue: Stryker received a report from the field indicating that a citation TMZF HA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot Ice Recalled by Altasource LLC dba Meta Labs LLC Due to Firm is not...
The Issue: Firm is not registered as a drug manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nice-En-Smooth Berry Burst Recalled by Altasource LLC dba Meta Labs LLC Due...
The Issue: Firm is not registered as a drug manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mega-Gen His Personal Lubricant Recalled by Altasource LLC dba Meta Labs LLC...
The Issue: Firm is not registered as a drug manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.