The Recall Desk

State

Kansas product recalls

72,984 recalls have nationwide distribution and so reach Kansas. 5,725 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total
5,725
Critical
1,046
Severe
1,228
Most recent
2026-09-16

Of the 5,725 recalls naming Kansas we have scored against our rubric, 1,046 (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 5,725 recalls whose distribution notice names Kansas specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5851–5875 of 78709

  • ModerateFDA (Devices)·Z-2298-2025·2025-08-20

    Ultra IABP catheter kits carry indications not reviewed by the FDA

    Insightra Ultra IABP Catheter Kits are being recalled because the device carries indications and compatibility claims not reviewed by the FDA, and its instructions are inconsistent with product training.

    Product
    Brand Name: Ultra IABP Catheter Kit Product Name: Ultra IABP Catheter Kit Model/Catalog Number: IMU7F-40, IMU7F-35, IMU7F-30, IMU7F-25, and IMU7F-20 Software Version: Not applicable Product Description: The Insightra Ultra IABP Catheter Kit is a 7 French catheter available wi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0445-2025·2025-08-20

    Lithium orotate 10 mg product recalled for failing labeled potency standard

    Lithium Orotate 10 mg distributed by Enjoy Nutrition, LLC is recalled nationwide because it does not meet its labeled potency, following a recall by the ingredient supplier.

    Product
    Lithium Orotate, 10MG, Distributed by Enjoy Nutrition, LLC. UPC#: 702730894033, 702730894057
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0442-2025·2025-08-20

    Lithium orotate 1 mg product recalled for failing labeled potency requirement

    Lithium Orotate 1 mg distributed by Enjoy Nutrition, LLC is recalled nationwide because it does not meet its labeled potency, following a recall by the ingredient supplier.

    Product
    Lithium Orotate, 1MG, Distributed by Enjoy Nutrition, LLC. UPC#: 717340952714
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2324-2025·2025-08-20

    Anorectal manometry kit outer label shows the manufacturing date as expiry

    Zvu Anorectal Manometry Procedure Kits are being recalled because the outer kit label carries an incorrect expiration date, with the manufacturing date used in its place. 8 kits are affected.

    Product
    Zvu Anorectal Manometry Procedure Kit, REF: HRAM-PROC-10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2288-2025·2025-08-20

    Prosthesis heads carry inconsistent size terminology and color coding on labeling

    Prosthesis Head B, 28 mm with 7 mm neck length, is being recalled because of inconsistent size terminology and colour coding used on the labeling. 46 units are affected.

    Product
    Prosthesis Head B, 28 mm, 7 mm neck length. Item Number: 198-828/04.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0443-2025·2025-08-20

    Lithium orotate 2.5 mg product recalled for failing labeled potency specification

    Lithium Orotate 2.5 mg distributed by Enjoy Nutrition, LLC is recalled nationwide because it does not meet its labeled potency. The action follows a recall by the ingredient supplier.

    Product
    Lithium Orotate, 2.5MG, Distributed by Enjoy Nutrition, LLC. UPC#: 719318414002; 709750005289
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0584-2025·2025-08-20

    Belsomra 10 mg tablets failed dissolution, which may delay sleep onset

    Belsomra (suvorexant) 10 mg tablets are being recalled because of failed dissolution specifications, with potential for delayed release of the drug and delayed onset of sleep. 51,320 cartons affected.

    Product
    BELSOMRA — BELSOMRA (SUVOREXANT)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2321-2025·2025-08-20

    Medication dispensing cabinets recalled after reports of delayed access during override workflow

    BD is recalling 6,076 Pyxis MedBank and MedBank Mini automated dispensing cabinets after reports of delayed access to medication caused by the override and Add Item workflow.

    Product
    Description/REF: BD PYXIS MEDBANK MINI 1FH-1FM/169-137, BD PYXIS MEDBANK MINI 4HM/169-113, BD PYXIS MEDBANK MINI 4HH/169-112, BD PYXIS MEDBANK MINI 3HH-1HM/169-111, BD PYXIS MEDBANK MINI 3HH-1FG/169-110, BD PYXIS MEDBANK MINI 2HM-1FM/169-109, BD PYXIS MEDBANK MINI 2HH-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0446-2025·2025-08-20

    Lithium orotate 20 mg product recalled after failing labeled potency testing

    Lithium Orotate 20 mg distributed by Enjoy Nutrition, LLC is recalled nationwide because it does not meet its labeled potency, following a recall by the ingredient supplier.

    Product
    Lithium Orotate, 20MG, Distributed by Enjoy Nutrition, LLC. UPC#: none
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V531000·2025-08-19

    Triumph Daytona 660 engines can fail from disrupted oil flow

    Triumph is recalling certain 2024-2025 Daytona 660 motorcycles because the engine may fail due to internal damage caused by a disruption of oil flow.

    Product
    TRIUMPH — TRIUMPH DAYTONA 660
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V530000·2025-08-18

    2026 RAM Trucks Instrument Panel Cluster Warning Light Malfunction

    Chrysler is recalling certain 2026 RAM 2500, 3500, 4500 Cab Chassis, and 5500 Cab Chassis vehicles because the instrument panel may display an incorrect brake system warning light, potentially failing to alert drivers to critical safety information.

    Product
    RAM — RAM 5500, 3500, 2500, 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25435·2025-08-14

    Drinkmate one litre carbonation bottles can explode during use

    Drinkmate 1L Carbonation Bottles are being recalled because they can explode during use. Eight reports include four resulting in lacerations, impact injuries and hearing damage. About 106,200 units affected.

    Product
    Drinkmate 1L Carbonation Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25437·2025-08-14

    ESR HaloLock wireless power bank batteries can overheat and ignite

    ESR HaloLock wireless power banks are being recalled because the lithium-ion battery can overheat and ignite. Nine fires and explosions caused about $20,000 in property damage.

    Product
    ESR HaloLock Wireless Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25432·2025-08-14

    Wolfgang Puck petite tea kettle infuser lids can fall off

    Wolfgang Puck Stainless Steel Petite Tea Kettles are being recalled because the infuser basket lid is loose and can fall off during use. Five of ten reports involved burns or scalding. About 40,000 units affected.

    Product
    Wolfgang Puck Stainless Steel Petite Tea Kettles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25431·2025-08-14

    Werner Multi-Max Pro ladder locking mechanisms can jam without fully locking

    Werner 20' and 24' Multi-Max Pro multi-purpose ladders are being recalled because the locking mechanism can jam and not fully lock. Eighteen falls and fourteen injuries reported. About 122,250 units affected.

    Product
    Werner 20' and 24' Multi-Max Pro Multi-Purpose Ladders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25434·2025-08-14

    Firefly Safe and Green fuel bottles have a non child-resistant applicator

    Firefly Safe & Green 32 oz fuel bottles are being recalled because the nozzle applicator is not child-resistant as required for hydrocarbons, and the fuel is incorrectly labeled "Non-Toxic".

    Product
    Firefly Safe & Green 32 oz. Fuel Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25430·2025-08-14

    Remington hair dryers lack an immersion protection device against electrocution

    Remington brand hair dryers, model D3190DCDN, are being recalled because they lack an immersion protection device, posing a risk of electrocution or shock if dropped into water. About 56,300 units affected.

    Product
    Hair Dryers sold under the "Remington" brand, model number D3190DCDN
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25436·2025-08-14

    Viewrail floating stair LED modules can overheat and melt

    Electronic LED modules used with floating stairs and rails are being recalled because the module can overheat and melt, posing a fire hazard. About 2,720 units are affected.

    Product
    Electronic LED modules used on Floating Stairs and Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25433·2025-08-14

    Children's spiral tower toys contain small balls banned for toddlers

    Three-tiered spiral children's tower toys are being recalled because the toy contains small balls and is intended for children under three, violating the small ball ban. About 260 units affected.

    Product
    Children's Spiral Tower Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2180-2025·2025-08-13

    BD Alaris pump infusion sets may perform outside established flow ranges

    BD Alaris Pump Infusion Sets are being recalled because the pump module used with them may perform outside the established ranges for flow rate, bolus accuracy and occlusion alarm timing.

    Product
    BD Alaris Pump Infusion Sets REF: 10013186, BD Alaris Pump Infusion Set, Back Check Valve, 3 SmartSite Y-sites LVP 60D DEHP FREE 3SS CV; REF: 2452-0007, BD Alaris Pump Infusion Set, 2 Back Check Valves, 3 SmartSite Y-sitesAS LVP 10D 3SS 2CV; REF: 2204-0007, BD Alaris Pum
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0394-2025·2025-08-13

    Member's Mark freeze dried fruit packs tested positive for Listeria monocytogenes

    Member's Mark Freeze Dried Fruit Variety Pack 15 count is being recalled after the firm received positive test results for Listeria monocytogenes during routine testing. 21,552 boxes affected.

    Product
    Member's Mark FREEZE DRIED FRUIT VARIETY PACK 15 COUNT 5-0.35OZ (10g) STRAWBERRY POUCHES 5-0.42OZ (12g) BANANA POUCHES 5-0.25 OZ (10g) APPLE POUCHES NET WT 5.6OZ (160g) NO ADDED SWEETENERS ONE INGREDIENT ONLY PER PACK UPC 1 93968 50900 2
    Category
    Food
    Distribution
    44 states