The Recall Desk

State

Kansas product recalls

73,737 recalls have nationwide distribution and so reach Kansas. 5,821 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total
5,821
Critical
1,053
Severe
1,485
Most recent
2026-10-28

Of the 5,821 recalls naming Kansas we have scored against our rubric, 1,053 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,485 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,821 recalls whose distribution notice names Kansas specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32926–32950 of 79558

  • ModerateFDA (Drugs)·D-0783-2020·2020-01-15

    Idelle Labs Recalls SURE 48 hr Anti-Perspirant for Labeling Error

    Idelle Labs is recalling SURE 48 hr Confidence Unscented Anti-Perspirant & Deodorant because the label lists an active ingredient that is not actually in the product.

    Product
    SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant, Net Wt. 2.6 oz (73g) NDC# 41595-5509-2 UPC 8 83484 71717 2 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0778-2020·2020-01-15

    Nextremity Solutions Recalls Stratum MDS Screws Due to Length Discrepancy

    Nextremity Solutions is recalling 86 Stratum MDS Screws because they are 2mm shorter than the length indicated on the package label.

    Product
    Stratum MDS Screw 3.5x50mm ST Part Number: STRM-MDS-3550ST
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0638-2020·2020-01-15

    Lupin Recalls Blisovi Fe 1.5/30 Tablets Due to Crumbling

    Lupin Pharmaceuticals is recalling Blisovi Fe 1.5/30 tablets because they crumble when removed from the blister pack.

    Product
    Blisovi Fe 1.5/30 (norethindrone acetate and ethinyl estradiol tablets USP and ferrous fumarate tablets 75mg), Rx Only, Distributed by: Lupin Pharmaceuticals Inc Baltimore, MD 21202, Manufactured for: Lupin Limited Pithampur 454775 INDIA 240875, NDC 68180-866-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0465-2020·2020-01-15

    Wayfare Butterscotch Pudding Recalled for Package Bloating and Off Flavors

    Wayfare Health Foods LLC is recalling Plant Based Butterscotch Pudding due to consumer complaints of package bloating, off flavors, and textural issues.

    Product
    Plant Based WayFare Butterscotch Pudding Organic Dairy Free, Item #1223. Net wt. 4 oz. There are 4/4 oz. cups per pack with cardboard overwrap. UPC 845681000372.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0794-2020·2020-01-15

    Baxter Recalls One-Link Needle-Free IV Connectors Due to Connection Force Issue

    Baxter Healthcare is recalling One-Link Needle-Free IV Connectors because some units require higher-than-expected force to connect securely to standard Luer adapters.

    Product
    ONE-LINK Needle-free IV Connector, Product Codes: 7N8300, 7N8301, 7N8310, 7N8330K, 7N8332K, 7N8334K, 7N8370K, 7N8371, 7N8375K, 7N8376K, 7N8377, 7N8378, 7N8390, 7N8391, 7N8399 - Product Usage: intended for single patient use with a vascular access device for the administration of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0786-2020·2020-01-15

    Idelle Labs Recalls SURE 48hr Anti-Perspirant Due to Labeling Error

    Idelle Labs is recalling SURE 48hr Confidence Unscented Anti-Perspirant because the label lists an active ingredient that is not actually in the product.

    Product
    SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant Net Wt 2.7 oz (76g) NDC# 41595-5513-2 UPC 8 83484 71794 3 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0784-2020·2020-01-15

    Idelle Labs Recalls SURE Antiperspirant for Undeclared Active Ingredient

    Idelle Labs is recalling SURE 48hr Confidence Nourishing Coconut Antiperspirant & Deodorant because the label lists an active ingredient that is not actually in the product.

    Product
    SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant & Deodorant Net Wt 2.6 oz (73g) NDC# 41595-5547-1 UPC 8 83484 31020 5 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·20056·2020-01-14

    Thompson's WaterSeal Aerosol Protectors Recalled for Fire Hazard

    The Thompson's Company is recalling about 852,000 aerosol cans of WaterSeal wood and masonry protectors because leaking propellant poses a fire hazard.

    Product
    Thompson's® WaterSeal® Waterproofing Wood Protector and Masonry Protector in Aerosol Cans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V012000·2020-01-13

    Toyota and Lexus Recall Vehicles for Fuel Pump Failure Risk

    Toyota is recalling approximately 1.8 million vehicles because a fuel pump failure could cause the engine to stall while driving, increasing crash risk.

    Product
    TOYOTA — TOYOTA, LEXUS TUNDRA, RC 350, CAMRY, ES350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V010000·2020-01-10

    Genuine Scooter Recalls 2020 Royal Alloy GT150 Due to Brake Rotor Defect

    Genuine Scooters is recalling 2020 Royal Alloy GT150 scooters because the front brake rotor may become uncentered, potentially causing a loss of braking and increasing crash risk.

    Product
    GENUINE SCOOTER — GENUINE SCOOTER ROYAL ALLOY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·002-2020·2020-01-10

    Culinary International Recalls Chicken Burritos Due to Undeclared Egg Allergen

    Culinary International is recalling approximately 626 pounds of frozen chicken burritos that actually contain eggs, an undeclared allergen. No illnesses have been reported.

    Product
    Ruiz Food Products, Inc. — Culinary International, LLC Recalls Chicken Burrito Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V011000·2020-01-10

    GM Recalls 2007-2008 Trucks for Air Bag Inflator Defect

    General Motors is recalling 2007-2008 Chevrolet Silverado and GMC Sierra trucks because front passenger air bag inflators may explode.

    Product
    GMC — GMC, CHEVROLET SIERRA 3500, SIERRA 2500, SILVERADO 2500, SILVERADO 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·20V007000·2020-01-09

    Ferrari Recalls 458 Italia and California for Air Bag Defect

    Ferrari is recalling 982 vehicles because front passenger air bag inflators may explode, posing a risk of serious injury or death.

    Product
    FERRARI — FERRARI 458 ITALIA, CALIFORNIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·20V008000·2020-01-09

    Nissan and Infiniti Recall Vehicles for Air Bag Inflator Defect

    Nissan is recalling specific 2001-2011 Nissan and Infiniti vehicles because front passenger air bag inflators may explode due to propellant degradation.

    Product
    INFINITI — INFINITI, NISSAN M45, QX4, I30, I35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20050·2020-01-09

    Holiday Travel Mugs Recalled Due to Fire Hazard in Microwaves

    Boston Warehouse Trading Corp. is recalling Holiday Travel Mugs sold at Meijer because metallic print can spark in microwaves, posing a fire hazard.

    Product
    Holiday Travel Mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20712·2020-01-09

    Little Bambino Tricycles Recalled for Lead Paint Violation and Poisoning Risk

    Thesaurus Global Marketing is recalling Little Bambino tricycles because lead levels in the paint and components exceed federal bans, posing a poisoning risk to young children.

    Product
    Little Bambino 4 in 1 canopy children's tricycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0633-2020·2020-01-08

    FDA Recalls Silver Bullet Male Enhancement Capsules for Undeclared Active Ingredient

    The FDA is recalling Silver Bullet male enhancement capsules because they contain an undeclared active ingredient (Sildenafil) and were marketed without an approved NDA/ANDA.

    Product
    Silver Bullet, Get Bigger and Harder, Works in Minutes, Lasts for Days, 10 male enhancement capsules in blister foil package, 725mg per capsule, Distributed by Silver Bullet Ltd, Golden Springs, CO, USA, UPC: 610877392698.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0746-2020·2020-01-08

    Thoratec HeartMate 3 Mobile Power Unit Recalled for Static Electricity Risk

    Thoratec Corp. is recalling HeartMate 3 Mobile Power Units because excessive static electricity can cause unrecoverable power loss, potentially reducing blood flow from the left ventricular assist system.

    Product
    HeartMate 3 Mobile Power Unit, REF 107754, UDI or GTIN: 00813024010883, and 107758, UDI or GTIN: 00813024010890, when connected to the HeartMate 3 Left Ventricular Assist System, REF 106524US, UDI or GTIN: 00813024013297, and 106524, UDI or GTIN: 00813024011712 - Product Usage…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0631-2020·2020-01-08

    American Health Packaging Recalls Ranitidine Syrup Due to NDMA Impurity

    American Health Packaging is recalling specific lots of Ranitidine Syrup because the presence of the NDMA impurity was detected in the product.

    Product
    Ranitidine Syrup (Ranitidine Oral Solution USP), 15 mg/mL, 150 mg/10 mL per cup, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio. (a) Case of 50 cups (NDC 60687-260-69) (b) Case of 40 cups (NDC 60687-260-23 (c) Unit Dose Cup (NDC 60687-260-69)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0765-2020·2020-01-08

    Villa Sistemi Medicali Recalls Apollo DRF X-ray Tables Due to Chain Failure

    Villa Sistemi Medicali is recalling seven Apollo DRF X-ray tables because the angulation chain may fail early due to metal fatigue.

    Product
    Apollo DRF, Model Number 9784220831 - Product Usage: The remote controlled table Apollo DRF is an X-ray equipment that allows to perform general radiographic and fluoroscopic examinations. The system is a fixed position type. The movements of the table and tube support are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0766-2020·2020-01-08

    Villa Sistemi Medicali Recalls Apollo EZ X-Ray Table Due to Chain Failure

    Villa Sistemi Medicali is recalling one Apollo EZ X-ray table because the angulation chain may fail early due to metal fatigue.

    Product
    Apollo EZ, Model Number 9784152036 - Product Usage: The Apollo EZ remote-controlled table is X-ray equipment that can be used to perform general radiographic and fluoroscopic examinations. The system is a fixed position type. The movements of the table and tube support are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0747-2020·2020-01-08

    Roche Recalls Accu-Chek Guide Blood Glucose Monitoring System Due to Power Issues

    Roche Diabetes Care is recalling Accu-Chek Guide Blood Glucose Monitoring Systems due to potential power issues. The recall affects 318,678 units distributed in the US and 35 other countries.

    Product
    Blood Glucose Monitoring System, Model Number 07400870001 ACCU-CHEK GUIDE SAMPLE KIT MG/DL - Product Usage: The Accu-Chek Guide Blood Glucose Monitoring System is intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and upper arm…
    Category
    Medical Device
    Distribution
    Distributed nationwide