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. 1,090 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,090 in last 12 months

Showing 9841–9860 of 28,538 recalls

Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s2 - Recalled by Nobel Biocare Procera...

The Issue: Not manufactured to specification

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for Recalled by...

The Issue: 3/4 AFT Straight Fill Tubes (227007) filled only 1/2 way instead of 3/4, may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% 13x75...

The Issue: VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% may show...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s4 - Recalled by Nobel Biocare Procera...

The Issue: Not manufactured to specification

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Philips North America Llc

Recalled Item: Philips Xper Flex Cardio (FC2010 Recalled by Philips North America Llc Due...

The Issue: Performance issues with the Xper Flex Cardio Physio Monitoring System...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s4 - Recalled by Nobel Biocare Procera...

The Issue: Not manufactured to specification

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s6 - Recalled by Nobel Biocare Procera...

The Issue: Not manufactured to specification

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿s3 - Product Recalled by Nobel Biocare...

The Issue: Not manufactured to specification

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number:...

The Issue: Some Artis zee ceiling systems show an increased abrasion of the cabling at...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Radiometer Medical ApS

Recalled Item: PIC070 Arterial Blood Sampler PICO70 - Product Usage: Preheparinized...

The Issue: Radiometer has become aware of an issue with PICO70 Arterial Blood Sampler....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS¿ Black Slides CATALOG #: J02316 - Product Usage: Recalled by...

The Issue: Delayed results. Ortho confirmed that two lots of VITROS Black Slides are...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· ROi CPS LLC

Recalled Item: Regard Dressing Change Tray Recalled by ROi CPS LLC Due to ChloraPrep...

The Issue: ChloraPrep applicators in the kit can grow organisms that can result in a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Bard Peripheral Vascular Inc

Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...

The Issue: Catheters may experience difficulty in flushing, infusion, and/or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Bard Peripheral Vascular Inc

Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...

The Issue: Catheters may experience difficulty in flushing, infusion, and/or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10 GAUGE DIRECT UNILATERAL STYLET (1 X DIAMOND 1 X Recalled by Zavation Due...

The Issue: Products distributed as sterile may not have been adequately sterilized

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Direct Access Diamond Tip Trocar Recalled by Zavation Due to...

The Issue: Products distributed as sterile may not have been adequately sterilized

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10 GAUGE DIRECT ACCESS DIAMOND TIP Recalled by Zavation Due to Products...

The Issue: Products distributed as sterile may not have been adequately sterilized

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10G COAXIAL CANNULA WITH TUOHY CONNECTION STERILE. For use in Recalled by...

The Issue: Products distributed as sterile may not have been adequately sterilized

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10 GAUGE CEMENT DELIVERY CANNULA Recalled by Zavation Due to Products...

The Issue: Products distributed as sterile may not have been adequately sterilized

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty System Recalled by Zavation Due to Products distributed as sterile...

The Issue: Products distributed as sterile may not have been adequately sterilized

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing