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. 2,616 recalls have been distributed to Kansas in the last 12 months.
Showing 4961–4980 of 50,117 recalls
Recalled Item: Baxter Spectrum Wireless Battery Modules A/B/G/N Recalled by Baxter...
The Issue: The Spectrum WBM may fail to auto-document infusion status information back...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectrum Wireless Battery Modules A/B/G/N Recalled by Baxter Healthcare...
The Issue: The Spectrum WBM may fail to auto-document infusion status information back...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WAVEWRITER ALPHA: Model: SC-1216 Recalled by Boston Scientific...
The Issue: Spinal Cord Stimulation (SCS) Implantable Pulse Generator (IPG) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo...
The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Firm has released a...
The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...
The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TiBrid Stand Alone Intervertebral Body Fusion Device Recalled by Omnia...
The Issue: Failure of fusion system instruments in the field.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TiBrid Stand Alone Intervertebral Body Fusion Device Recalled by Omnia...
The Issue: Failure of fusion system instruments in the field.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: CLEARCUT SAFETY INTREPID DB Recalled by Alcon...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: 25+ TTL PLUS VPAK 20000CPM BWV Model/Catalog Number: Recalled...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: CLEARCUT SATINSLIT FULL HANDLE2.75MM AN...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: 25+ CMB PAK 10K CPM Recalled by Alcon Research LLC Due to...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: TOTAL PLUS Recalled by Alcon Research LLC Due to Alcon has...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray System with Software...
The Issue: Potential Loss of Imaging (X-ray) Functionality and/or Longer Time to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: ClearCut Sideport Knife Dual Bevel 1.2mm...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: CLEARCUT SLIT FULL HANDLE2.6MM ANG DUAL Recalled...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: CLEARCUT SLIT FULL HANDLE2.75MM ANG DUA Recalled...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: A-OK 19G V-LANCE FULL HANDLE1.6MM SATIN Recalled...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.