Kansas recalls
4277 federal recalls on file affecting Kansas - 360 Kansas-specific plus 3917 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-16CPSCShenzhen Gudebo Technology Co. Ltd., of ChinaNationwideLiizousuda paint thinner recalled for child poisoning risk
The paint thinner contains low-viscosity petroleum distillates, which must be in child-resistant packaging, as required by the?Poison Prevention Packaging Act. The bottles are not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children. Additionally, petroleum distillates can get into the lungs, causing chemical pneumonia and/or pulmonary damage, which can be fatal.
- 2026-07-16CPSCPanasonic Manufacturing (Xiamen) Co., Ltd, of Xiamen, Fujian, ChinaNationwidePanasonic toaster oven recalled for shock and fire risk
The power cord insulation can be insufficient due to a protective fiberglass sleeve not covering it adequately, posing a risk of shock and/or fire hazard.
- 2026-07-16CPSCShenzhen Dami Trading Co., Ltd., dba Delightmi, of ChinaNationwideOitnlaughter finger lights recalled for battery ingestion risk
The recalled finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.
- 2026-07-09CPSCGreenworks North America, LLC, dba Greenworks Tools, of Mooresville, North CarolinaNationwideGreenworks Tools Recalls 24V and 48V Kobalt Yard Power Tools with USB-C Batteries Due to Risk of Serious Injury from Fire Hazard
Charging the lithium-ion batteries through the USB-C port, while the batteries are inserted in the yard power tools can cause the batteries to short-circuit, posing a risk of serious injury from fire hazard.
- 2026-07-09CPSCiDecoz Inc. dba Flaunt, of Brooklyn, New York and Case-Mate, of Atlanta, GeorgiaNationwideFlaunt MagSafe Battery Charger recalled for fire risk
The lithium-ion battery in the recalled power banks (chargers) can overheat and ignite, posing a risk of serious injury or death from fire and burn hazards.
- 2026-07-09CPSCZhangzhoushi Jingqu Trading Co., Ltd., dba Wonder Stone Toys, of ChinaNationwideWonderStone infant walkers recalled for fall hazard
The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a risk of serious injury or death due to a fall hazard.
- 2026-07-09CPSCshenzhenshiyuezhangwangluokejiyouxiangongsi (Shenzhen Yuezhang Network Technology Co., Ltd.), doing business as YUEZHANG, of ChinaNationwideMoodooy bed rails recalled for entrapment risk
The recalled bed rails violate the mandatory standard for?adult portable bed rails?because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation.?In addition, the bed rails do not bear the required hazard warning labels.
- 2026-07-09CPSCJomani International Inc., of Monterey Park, CaliforniaNationwideBBRKIN and MouTec gun safes recalled for unlock risk
The biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death.
- 2026-07-09CPSCBest Buy Purchasing LLC, of Richfield, MinnesotaNationwideInsignia gas ranges recalled for fire hazard risk
The recalled ranges' front-mounted knobs can be activated accidentally by humans or pets, posing a risk of serious injury from a fire hazard.
- 2026-07-09CPSCConair LLC, of Stamford, Connecticut, dba CuisinartNationwideCuisinart Propel+ gas grill recalled for glass shatter risk
The tempered glass window in the pizza oven can shatter during use, posing a risk of serious injury from laceration hazard.
- 2026-07-08FDA-DeviceZimmer BiometClass IINationwideZimmer Surgical tourniquet hoses recalled for sterility breach
Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insignificant extension of surgery to find another readily available device.
- 2026-07-08FDA-DeviceZimmer BiometClass IINationwideBrand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Dual Hose with CPC Connectors Model/Catalog Number: 60-1812-101-00 Software Version: N/A Product Description: Dual Sterile Extension Hose with PLC Connector Component: N/A
Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insignificant extension of surgery to find another readily available device.
- 2026-07-08FDA-DeviceW L Gore & Associates, Inc.Class IINationwideGORE TAG thoracic endoprosthesis recalled for catheter separation
Due to catheter separation
- 2026-07-08FDA-DeviceMasimo CorporationClass IINationwideMasimo Radius VSM cuff recalled for false alarms and rough edges
Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal heart rate patients, which may distract clinicians away from management of true positive alarms, which could delay treatment; 2) Small and medium size blood pressure cuffs may contain rough edges, may result in skin irritation/redness.
- 2026-07-08FDA-DeviceMasimo CorporationClass IINationwideMasimo Radius VSM ECG set recalled for false alarms and cuff irritation
Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal heart rate patients, which may distract clinicians away from management of true positive alarms, which could delay treatment; 2) Small and medium size blood pressure cuffs may contain rough edges, may result in skin irritation/redness.
- 2026-07-08FDA-DeviceLaborie Medical Technologies CorpClass IINationwideLaborie Solar GI System recalled for moisture accumulation risk
Under extended clinical use conditions (e.g., long duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing or at the hydrophobic filter and waterproof pressure sensors. Accumulated moisture may affect airflow or pressure measurement performance if not properly removed.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Access Systems biopsy trays recalled for defective lidocaine
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Provena Midline Catheters recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerPICC catheters recalled for lidocaine quality issue
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Groshong NXT catheter recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerPICC Provena catheters recalled for defective lidocaine
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerMidline Catheter recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerMidline Catheter recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Power-Trialysis dialysis catheters recalled for lidocaine defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Power-Trialysis dialysis catheters recalled for lidocaine defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerPICC SV catheters recalled for lidocaine defects
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerPICC SOLO HF Catheter recalled for defective lidocaine
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard DuoGlide dialysis catheter recalled for defective lidocaine
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Poly Midline Catheter recalled for lidocaine manufacturing defects
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Access Systems drainage trays recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
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