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. 2,566 recalls have been distributed to Kansas in the last 12 months.
Showing 11921–11940 of 28,538 recalls
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A3 C17/5 - ceramic for dental...
The Issue: Restorations crack during the sintering process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A1 C17/5 -ceramic for dental...
The Issue: Restorations crack during the sintering process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiovascular Monitoring Device accessory - Product Usage: The chest...
The Issue: The labeling of the Philips Chest Pneumograph does not include a statement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Zenition 70 Recalled by Philips North America, LLC Due to When...
The Issue: When strain relief is lost at the stand side of the Stand MVS Trolley Cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Zenition 50 Recalled by Philips North America, LLC Due to When...
The Issue: When strain relief is lost at the stand side of the Stand MVS Trolley Cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Processor Board PCA Replacement Kits 453563478461 Recalled by...
The Issue: Damaged ESD bags used for storing components in Processor PCA Replacement Kits
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris PCEA Administration Set Recalled by BD SWITZERLAND SARL Due to The...
The Issue: The products have the potential to leak between the connection of the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.