The Recall Desk

State

Kansas product recalls

72,820 recalls have nationwide distribution and so reach Kansas. 5,723 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total
5,723
Critical
1,045
Severe
1,228
Most recent
2026-09-02

Of the 5,723 recalls naming Kansas we have scored against our rubric, 1,045 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,228 (21%) are Severe.

Which agencies issued them

These figures cover only the 5,723 recalls whose distribution notice names Kansas specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

401–425 of 78543

  • ModerateFDA (Devices)·Z-2838-2026·2026-08-12

    Boston Scientific Radial Jaw 4 Biopsy Forceps Recalled Due to Sterile Barrier Breach Risk

    Boston Scientific Corporation is recalling specific Radial Jaw 4 Standard Capacity Biopsy Forceps because there is a potential for a breach in the sterile barrier of the device packaging.

    Product
    Radial Jaw 4 Standard Capacity Biopsy Forceps with the following descriptions and UPN: 1. Radial Jaw 4 SC 240cm Box 20; Outer Box UPN: M00513401; Inner Box UPN: M00513400. 2. Radial Jaw 4 SC 240cm Box 40; Outer Box UPN: M00513402; Inner Box UPN: M00513400. 3. Radia
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2896-2026·2026-08-12

    5-PLASMA Bivalirudin Control Model 5D-44905 Recalled Due to Stability Issues

    Aniara Diagnostica LLC is recalling 5-PLASMA Bivalirudin Control (Model 5D-44905) due to stability issues that may cause degradation of measurable bivalirudin.

    Product
    5-PLASMA Bivalirudin Control, Model Number 5D-44905
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1223-2026·2026-08-12

    Pumpkin Tree Peter Rabbit Organics Banana and Strawberry Fruit Puree Recalled for Foreign Objects

    PT Organics Limited is recalling certain Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree pouches due to the potential presence of thin, soft plastic strands.

    Product
    Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree, 4oz/113g pouch, UPC 815367010780, PTO Item 10720. Distributed by: PT Organics Ltd, 333 South State St, Suite V-142, Lake Oswego, OR 97034. Product is pasteurized blend of banana and strawberry purees sold in si
    Category
    Food
    Distribution
    23 states
  • ModerateFDA (Devices)·Z-2905-2026·2026-08-12

    COAPTIUM CONNECT peripheral nerve repair device recalled due to inaccurate shelf life labeling

    The FDA is recalling the COAPTIUM CONNECT peripheral nerve repair device because its shelf life was previously overstated, which could cause device failure during surgery.

    Product
    Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number: NCOCO3010 Software Version: N/A Product Description: In situ polymerizing peripheral nerve repair device Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2895-2026·2026-08-12

    Aniara 5-PLASMA Bivalirudin Calibrator Recalled for Stability Issues

    Aniara Diagnostica LLC is recalling 7 units of 5-PLASMA Bivalirudin Calibrator due to stability issues that cause degradation of measurable bivalirudin.

    Product
    5-PLASMA Bivalirudin Calibrator, Model Number 5D-46905
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2881-2026·2026-08-12

    Siemens Tricyclic Antidepressant Calibrator/Controls Recall Lot U2

    Siemens Healthcare Diagnostics is recalling Lot U2 of its Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls due to an out-of-specification sodium azide concentration. The recall affects 494 units in the US and 114 units overseas, distributed nationwide and internationally.

    Product
    Syva Emit tox Serum Tricyclic Antidepressant Calibrator/Controls SMN 10445390 Catalog No. 7C219UL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2910-2026·2026-08-12

    Blom-Singer Voice Prosthesis Recalled Due to Incorrect Labeling

    Freudenberg Medical recalls 40 Blom-Singer Classic Indwelling Voice Prostheses due to labeling errors that could cause confusion about product contents.

    Product
    Blom-Singer Classic Indwelling Voice Prosthesis, 16Fr/10 mm REF: 1610-LF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2908-2026·2026-08-12

    COAPTIUM CONNECT medical device shelf life recalibration recall

    TISSIUM SA is recalling COAPTIUM CONNECT devices because their original 36-month shelf life was not supported by real-time data, requiring relabeling to a 26-month shelf life to prevent potential device failure during surgery.

    Product
    Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number: NCOCO6010 Software Version: N/A Product Description: In situ polymerizing peripheral nerve repair device Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V523000·2026-08-10

    Daimler Recalls 2024-2027 Thomas Built Buses Saf-T-Liner C2 for Fuel System Defect

    Daimler Trucks North America is recalling 2024-2027 Thomas Built Buses Saf-T-Liner C2 transit buses because the fuel tank cage and fuel system mounting may be incompatible, increasing the risk of a fire during a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V520000·2026-08-10

    Blue Bird Recalls 2023-2027 Vision Transit Buses for Wiring Defect

    Blue Bird is recalling 2023-2027 Vision Transit Buses because a damaged 12V power wire may short circuit, potentially disabling safety lights and increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V522000·2026-08-10

    Thomas Built Buses Recalls Saf-T-Liner C2 School Buses for Fuel System Defect

    Daimler Trucks North America is recalling 2024-2027 Thomas Built Buses Saf-T-Liner C2 school buses because incompatible fuel tank components may cause a fuel leak and fire during a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V519000·2026-08-10

    Blue Bird Recalls Vision School Buses Over Electrical Short Circuit Risk

    Blue Bird is recalling certain Vision School Buses because a 12V power wire may short circuit, disrupting rear lighting or warning lights and increasing crash risk. Dealers will repair free.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS, VISION SCHOOL BUS (ELECTRIC)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V521000·2026-08-10

    Marion Recalls 2025 Pumper Fire Engines Due to Display Unit Failure

    Marion Body Works is recalling 2025 Pumper fire engines because a display unit may fail, preventing the activation of emergency lights and firefighting equipment.

    Product
    MARION — MARION PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·015-2026·2026-08-08

    City Foods, Inc. Recalls Pastrami and Corned Beef Due to Listeria Risk

    City Foods, Inc. is recalling approximately 3,215 pounds of ready-to-eat pastrami and corned beef products because they may be contaminated with Listeria monocytogenes.

    Product
    City Foods, Inc./Bea's Best Corned Beef — City Foods, Inc. Recalls Ready-To-Eat Pastrami and Corned Beef Products Due To Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-08082026-01·2026-08-08

    Meat and poultry products containing recalled jalapeños may contain Salmonella

    The USDA FSIS is issuing a public health alert for various meat and poultry products that contain FDA-regulated jalapeños potentially contaminated with Salmonella.

    Product
    FSIS Issues Public Health Alert for Various Meat and Poultry Products Containing FDA-Regulated Jalapeños That Have Been Recalled Due To Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalCPSC·26664·2026-08-06

    BUSOHA Magnetic Fidget Slider Toys Recalled Due to Magnet Ingestion Risk

    BUSOHA is recalling approximately 2,186 Magnetic Fidget Slider Toys sold on Amazon because they can release magnets that pose a serious injury or death risk if swallowed.

    Product
    BUSOHA Magnetic Fidget Slider Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·26675·2026-08-06

    Courant Spliced Kalimba Climbing Ropes Recalled Due to Fall Hazard Risk

    Wichard Groupe North America is recalling Courant Spliced Kalimba climbing ropes because the spliced ends can fail, creating a risk of serious injury or death from falls.

    Product
    Courant Spliced Kalimba Climbing Ropes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·26667·2026-08-06

    PIXLABBY Silicone Magnetic Fidget Sliders Recalled Due to Magnet Ingestion Risk

    PIXLABBY is recalling its silicone magnetic fidget sliders because they can release high-powered magnets that pose a serious injury or death risk if swallowed by children.

    Product
    PIXLABBY Silicone Sensory Magnetic Fidget Sliders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·26677·2026-08-06

    Apeks Second Stage Scuba Regulators Recalled Due to Drowning Hazard

    HEAD Watersports is recalling Apeks second stage scuba regulators because they can restrict airflow at depths exceeding 45 meters, posing a risk of serious injury or death.

    Product
    Apeks Second Stage Scuba Regulators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·26670·2026-08-06

    EEMB Lithium-ion Coin Battery Chargers Recalled Due to Ingestion Risk

    A2batt is recalling EEMB Lithium-ion Coin Battery Chargers because the included batteries can be easily accessed by children, posing a risk of serious injury or death if swallowed.

    Product
    EEMB Lithium-ion Coin Battery Chargers with Rechargeable 2032 Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26668·2026-08-06

    Liuqibax Adult Bed Rails Recalled Due to Entrapment and Asphyxiation Risks

    Liuqibax is recalling approximately 12,000 adult portable bed rails sold on Amazon because they violate mandatory safety standards and pose entrapment and asphyxiation hazards.

    Product
    Liuqibax Adult Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V518000·2026-08-06

    Jayco Recalls 2027 Fifth Wheel Trailers Due to Auto Leveling Jack Defect

    Jayco is recalling 2027 Eagle and Heartland Sundance fifth wheel trailers because auto leveling jacks may lower during transit, increasing crash risk.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, HEARTLAND EAGLE, SUNDANCE FIFTH WHEEL, EAGLE SLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26671·2026-08-06

    Little Rawr Silicone Pull String Teething Toys Recalled Due to Choking Hazard

    Little Rawr Silicone Pull String Teething Toys are being recalled because the silicone strings are too long and thin, posing a choking and respiratory distress risk. One report of a child experiencing respiratory distress has been received.

    Product
    Little Rawr Silicone Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide