The Recall Desk

State

Kansas product recalls

20,096 recalls have nationwide distribution and so reach Kansas. 0 additional recalls listed Kansas specifically in their distribution scope.

About recalls in Kansas

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Kansas consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

6726–6750 of 20096

  • SevereNHTSA·24V433000·2024-12-06

    2025 Kenworth and Peterbilt Trucks Steering Linkage Defect

    PACCAR is recalling 2025 Kenworth and Peterbilt trucks due to improperly heat-treated ball studs in steering assemblies that may break, causing loss of steering control.

    Product
    KENWORTH — 2025 KENWORTH W990
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25056·2024-12-05

    Anker Soundcore and PowerConf Bluetooth speakers recalled for fire hazard

    Anker is recalling about 69,000 Soundcore and PowerConf Bluetooth speakers sold on Amazon in 2023 due to overheating lithium-ion batteries. The firm received 33 reports of incidents, including fires and one minor burn injury.

    Product
    Anker Soundcore (A3102) and PowerConf Bluetooth (A3302) Speakers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25058·2024-12-05

    NetZero High Bay LED Fixtures Recalled Due to Fire Hazard

    NetZero USA is recalling about 13,000 High Bay LED light fixtures due to plastic pin degradation that can cause the LED board to come loose and catch fire. Seven burning incidents have been reported with no injuries.

    Product
    High Bay LED light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25061·2024-12-05

    Belkin Power Bank Recalls Due to Fire Hazard from Battery Overheat

    Belkin is recalling about 4,000 BoostCharge Pro wireless charger power banks due to a fire hazard from overheating lithium-ion batteries. One unit caught fire and damaged a house.

    Product
    Belkin BoostCharge Pro Fast Wireless Charger Power Banks 10K
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25702·2024-12-05

    Polaris Recalls 2024 Ranger and Bobcat Off-Road Vehicles for Seat Belt Defect

    Polaris recalled about 2,500 Model Year 2024 Ranger and Bobcat vehicles with a defective passenger side seat belt anchor weld. Consumers should immediately stop carrying passengers and contact an authorized dealer for free repair.

    Product
    Model Year 2024 Ranger Recreational Off-Road Vehicles (ROVs) and ProXD and Bobcat Utility Task Vehicles (UTVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25057·2024-12-05

    Scented candles recalled due to fire and laceration hazards

    Vacation Inc. recalls about 13,000 units of Black Label Scented Candles due to flame overheat causing glass breakage and creating fire and laceration risks. No injuries have been reported, but consumers should stop using the product immediately.

    Product
    The Legendary 'VACATION' by Vacation Black Label Scented Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V365000·2024-12-05

    Loose Seat Belt Attachment in Winnebago and Itasca Motorhomes

    Winnebago and Itasca recall certain 2020-2023 motorhomes due to improperly tightened seat belt attachments that may fail to restrain occupants in a crash. Dealers will tighten fasteners free of charge.

    Product
    WINNEBAGO — 2021 WINNEBAGO INSPIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25060·2024-12-05

    Fireproof Gun Safes Recalled for Locking Mechanism Failure Risk

    Academy Sports + Outdoors is recalling about 6,100 Redfield 12- and 18-gun fireproof safes because mechanical locking plates can fail, potentially allowing unauthorized access. No injuries have been reported.

    Product
    Redfield 12- and 18-Gun Fireproof Safes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25703·2024-12-05

    Polaris RZR XP Off-Road Vehicles Recalled Due to Fire Hazard

    Polaris is recalling about 21,000 RZR XP 1000 and XP 4 1000 recreational off-road vehicles because the battery terminal cover can be damaged by the seat base, exposing the battery post and creating a fire hazard. No injuries have been reported.

    Product
    Model Year 2024-2025 RZR XP 1000 and XP 4 1000 ROVs
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25059·2024-12-05

    QVC recalls 1.1 million Temp-tations oven gloves due to burn hazard

    QVC is recalling about 1.1 million pairs of Temp-tations oven gloves that can fail to protect from heat, causing a burn hazard. The company received 162 reports of insufficient protection, including 92 reports of minor burns.

    Product
    Temp-tations Oven Gloves
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0328-2025·2024-12-04

    Hologic BioZorb Radiographic Marker Recalled Due to Serious Injury Reports

    Hologic has recalled 12,710 BioZorb Markers nationwide after receiving reports of serious complications including infection, device migration, and device erosion. The FDA classified this as a Class I recall.

    Product
    BioZorb Marker. Radiographic soft tissue marker.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V289000·2024-12-04

    2022 Forest River Columbus fifth wheel: missing riser tube risks tire damage and crashes

    Forest River is recalling approximately 137 2022 Columbus fifth wheel vehicles because the riser tube between the axle hangers was not installed. This creates inadequate tire clearance, risking tire puncture and vehicle crashes.

    Product
    FOREST RIVER — 2022 FOREST RIVER COLUMBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0200-2025·2024-12-04

    Griddle Waffles Recalled for Potential Listeria Contamination

    Treehouse Foods is recalling approximately 9.9 million cases of Krusteaz griddle waffles and related products due to potential Listeria monocytogenes contamination. Products with batch codes starting with 2C and best-by dates through October 11, 2025 are included.

    Product
    KRUSTEAZ 1/2.5lb GRDL WFL BLGN 7-KRSTZ UPC 068615115168 KRUSTEAZ 1/11.25oz GRDL WFL BLGN-KRSTZ UPC BAKERS SOURCE 1/11.25oz GRDL WFL BLGN-BKRSC UPC 089356143562 GORDON FOOD SERVICE 3/2.5lb GRDL WFL BLGN 7-GDNFS UPC 093901310323
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0571-2025·2024-12-04

    Essenz HLM Heart-Lung Machines May Fail Due to Software Defect

    The recalled Essenz HLM heart-lung machines (38 units) may experience GUI display failures and sensor deactivation. This can lead to hypoxia and hypoperfusion.

    Product
    Essenz HLM (Heart-Lung Machine), REF: 49-00-10, with Software
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0531-2025·2024-12-04

    AMS Artificial Urinary Sphincter Balloon Mislabeled With Wrong Component

    Boston Scientific recalls 52 mislabeled AMS Artificial Urinary Sphincter balloons that may contain a Control Pump instead of the labeled Pressure Regulating Balloon component.

    Product
    AMS Artificial Urinary Sphincter Pressure Regulating Balloon 61-70 cm H2O
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0526-2025·2024-12-04

    Karl Storz surgical instruments recalled for sterility barrier defect

    Karl Storz Endoscopy has recalled 105 surgical instruments with holes in their sterility barriers. The defect may compromise product sterility; affected devices were distributed nationwide and internationally.

    Product
    4.5 x 180 mm REF 28208BKS Aggressive Cutter, sterile, 6x 3.5 x 70 mm REF 28206CBS Full Radius Resector, sterile, 6x 5.5 x 120 mm REF 28205NDS Aggr. Pro Line Shaver Blade, sterile, 6x 5.5 x 120 mm REF 20205FDS Round Burr, sterile, 6x 6.5 x 120 mm REF 28205HES, Aggressi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0171-2025·2024-12-04

    Simple Truth Griddle Waffles Recalled for Potential Listeria Contamination

    Treehouse Foods is recalling Simple Truth Griddle Waffle Blueberry products nationwide due to potential Listeria monocytogenes contamination. Consumers should discard affected packages.

    Product
    SIMPLE TRUTH 12/11.3oz GRDL WFL BLBRY GF-SMPTR UPC 011110105509
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0534-2025·2024-12-04

    Medline Shoulder Repair Pack-LF Recalled for Incorrect Surgical Components

    Medline is recalling Shoulder Repair Pack-LF surgical kits (lot 24ABO552) due to incorrect needle type/size and suture diameter/length in some packages. No patient injuries have been reported.

    Product
    Medline Shoulder Repair Pack-LF, REF DYNJ82607, 2 kits/case, sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0162-2025·2024-12-04

    H-E-B and Central Market Griddle Waffles Recalled for Listeria Risk

    H-E-B and Central Market brand griddle waffles with apple cinnamon are being recalled nationwide due to potential Listeria monocytogenes contamination affecting 9,907,389 cases.

    Product
    H-E-B 12/9oz GRDL WFL APL CIN ORG-HEBUT UPC 041220708376 CENTRAL MARKET 12/9oz GRDL WFL APL CIN ORG - CTMKT UPC 041220655748
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·24V267000·2024-12-04

    Ford Bronco Sport Control Module Failure May Disable Drive Power

    Ford is recalling Bronco Sport and Maverick models due to control module defects that may fail to detect low battery charge, potentially disabling drive power and increasing crash risk. Dealers will provide free recalibration.

    Product
    FORD — 2022 FORD BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0530-2025·2024-12-04

    AMS Artificial Urinary Sphincter Control Pump: Mislabeled Packaging Recall

    Boston Scientific recalled 16 units of AMS Artificial Urinary Sphincter Control Pumps due to mislabeled packaging where devices labeled as Pressure Regulating Balloons actually contained Control Pumps.

    Product
    AMS Artificial Urinary Sphincter Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0549-2025·2024-12-04

    Offset Cup Impactor Surgical Instruments Recalled for Weld Fracture

    INCIPIO DEVICES is recalling 100 units of Offset Cup Impactor surgical instruments (Lot 24A0087) because the TIG weld does not meet specifications and has fractured. These instruments are used in hip surgery to position acetabular cup implants.

    Product
    Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used to position and place acetabular sup implants.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0152-2025·2024-12-04

    Treehouse Foods Recalls Frozen Waffles for Potential Listeria Contamination

    Treehouse Foods is recalling BREAKFAST BEST frozen griddle waffles nationwide due to potential Listeria monocytogenes contamination. Approximately 9.9 million cases are affected; consumers should not eat the product.

    Product
    BREAKFAST BEST 12/12.3oz MXD CS GRDL WFL PMPKN/CINN-BKBST UPC 4061463257208
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0536-2025·2024-12-04

    Philips Achieva TX Interventional Coil 3.0T Recalled for Patient Safety Risk

    Philips recalls the Achieva TX Interventional Coil 3.0T (5,231 units) for a potential safety issue that may harm patients during MRI scan preparation or procedures.

    Product
    Achieva TX Interventional Coil 3.0T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0510-2025·2024-12-04

    Medline Epidural Catheter Kits Recalled Due to Connector Position Defect

    Medline is recalling over 5,900 epidural catheter kits because the connectors may not open fully, preventing proper catheter insertion. The recall affects units distributed nationwide and internationally.

    Product
    MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE, REF EPICATH19 2) 20G EPI CATH SINGLE STERILE, REF EPICATH20
    Category
    Medical Device
    Distribution
    Distributed nationwide