The Recall Desk

State

Kansas product recalls

73,597 recalls have nationwide distribution and so reach Kansas. 5,756 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total
5,756
Critical
1,053
Severe
1,480
Most recent
2026-10-14

Of the 5,756 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 1,480 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,756 recalls whose distribution notice names Kansas specifically. The 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26226–26250 of 79353

  • HighFDA (Food)·F-0698-2021·2021-06-30

    Clio Vanilla Greek Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Vanilla Greek Yogurt Bars (50g x 10 pack, UPC 861703000106) due to the possible presence of metal fragments. The recall affects 196,863 cases distributed nationwide with best-by dates between February 14, 2021 and June 27, 2021.

    Product
    Clio Vanilla Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack. UPC code: 861703000106
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1948-2021·2021-06-30

    Surgical instrument trays recalled for potential flaking metal and brown spots

    Medical Action Industries recalls General Purpose Instrument Trays due to potential flaking metal and brown spots on hemostats. These defects could contaminate surgical instruments.

    Product
    Medical Action INDUSTRIES INC., General Purpose Instrument Tray, REF 61209
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0689-2021·2021-06-30

    Clio Expresso Greek Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Expresso Greek Yogurt Bars due to the possible presence of metal fragments. The recall affects 6,733 cases distributed nationwide with best-by dates between February 14, 2021 and July 11, 2021.

    Product
    Clio Expresso Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC code: 867155000244
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1950-2021·2021-06-30

    Econocare Plus Waffle Overlay Recalled for Bodily Fluid Contamination

    EHOB, Inc. is recalling 70 units of the Econocare Plus Waffle Overlay due to trace amounts of dried bodily fluids that may expose patients and healthcare providers to contaminants.

    Product
    Econocare Plus Waffle Overlay- Intended for use as a medical device to aid in the prevention and treatment of pressure injuries or bed sores and general comfort. Product Code: 1025ECP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1941-2021·2021-06-30

    OptiChamber Diamond Spacer Recalled Due to Temperature Exposure During Shipping

    Cardinal Health is recalling 375 OptiChamber Diamond Spacer devices due to temperature exposure during shipping that may cause inaccurate medication delivery results. Affected devices were distributed to Florida, Georgia, and South Carolina.

    Product
    OPTICHAMBER DIAMOND SPACER WITH LARGE MASK Item Number: 4742326
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0640-2021·2021-06-30

    Metformin Hydrochloride Tablets Recalled for NDMA Contamination

    Viona Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets 750 mg due to detection of N-Nitrosodimethylamine (NDMA) levels exceeding acceptable daily intake limits.

    Product
    METFORMIN HYDROCHLORIDE — METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1951-2021·2021-06-30

    LEGION Knee Prosthesis Component Recalled for Manufacturing Surface Damage

    Smith & Nephew is recalling 5 units of a knee prosthesis component due to surface damage from a manufacturing error. The affected lot was distributed in specific U.S. states.

    Product
    LEGION Posterior Stabilized OXINIUM Femoral Component, REF 71421216, Size 6, Left, Nonporous Femoral Component, A/P 65.5 MM, M/L 73 MM, For Cemented Use Only, ZR-2.5NB,Sterile. Knee prosthesis component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1936-2021·2021-06-30

    OneTouch Ultra Blue test strips recalled for temperature exposure damage

    Cardinal Health is recalling 5,356 boxes of OneTouch Ultra Blue test strips after units were exposed to freezing temperatures during shipping, which may cause inaccurate glucose readings.

    Product
    ONETOUCH ULTRA BLUE TEST STRIPS 100 COUNT Item Number: 2990174
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1927-2021·2021-06-30

    Cardiac assessment system may display test reports in wrong patient records

    GE Healthcare's Case Cardiac Assessment System and CardioSoft diagnostic application may display one patient's cardiac test report in another patient's medical record under certain conditions. No patient injuries have been reported.

    Product
    Case Cardiac Assessment System for Exercise Testing and CardioSoft Diagnostic System Exercise Stress Testing ECG application
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0686-2021·2021-06-30

    Clio Vanilla Greek Yogurt Mini Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Vanilla Greek Yogurt Mini Bars due to the possibility of metal fragments in the product. Consumers should not consume affected yogurt bars.

    Product
    Clio Vanilla Greek Yogurt Mini Bars wrapped in a Chocolate Coating 6.2oz pouch x 6 pouches per case, UPC: 854021008077
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1932-2021·2021-06-30

    AeroChamber PLS Spacer Recalled Due to Temperature Exposure During Shipping

    Cardinal Health is recalling AeroChamber PLS spacers exposed to freezing temperatures during shipping, which may cause inaccurate drug delivery results. Affected units shipped between February and March 2021 in Florida, Georgia, and South Carolina.

    Product
    AEROCHAMBER PLS W/MASK LRG BLU Item Number: 1496033
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0693-2021·2021-06-30

    Clio Peach Less Sugar Yogurt Bars recalled for possible metal fragments

    Clio LLC is recalling Clio Peach Less Sugar Yogurt Bars due to the possible presence of metal fragments in the product. The 10-pack boxes with best buy dates between 2/7/2021 and 6/20/2021 were distributed nationwide.

    Product
    Clio Peach Less Sugar Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC code: 854021008213
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0690-2021·2021-06-30

    Clio Honey Greek Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Honey Greek Yogurt Bars due to the possibility of metal fragments in the product. The recall affects 5,423 cases distributed nationwide with best-by dates between March 7, 2021 and July 11, 2021.

    Product
    Clio Honey Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC code: 861703000168
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V492000·2021-06-30

    2021 Volkswagen Jetta Air Bag Control Module Welding Defect Recall

    Volkswagen is recalling 2020-2021 Jetta vehicles because the air bag control module was welded in an incorrect position. This can cause air bags to deploy improperly during a crash or deploy unexpectedly, increasing injury risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0697-2021·2021-06-30

    Clio Greek Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Vanilla and Strawberry Club pack Greek Yogurt Bars nationwide due to the possibility of metal fragments in the product. Consumers should not eat the affected bars.

    Product
    Clio Vanilla / Strawberry Club pack Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 12 , 16pc tray, 24g x 24 (12pc tray), 55g x 16 (8pc tray). UPC codes: 854021008121, 854021008138, and 854021008022
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0692-2021·2021-06-30

    Clio Mixed Berry Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Mixed Berry Less Sugar Yogurt Bars due to possible metal fragments in the product. Consumers should not eat the affected bars and should contact the company or return them to the retailer.

    Product
    Clio Mixed Berry Less Sugar Yogurt Bars wrapped in a Chocolate Coating 10 Clio Retail 10-pack, UPC code: 854021008190
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1937-2021·2021-06-30

    OneTouch Ultrasoft Lancets recalled due to temperature exposure during shipping

    Cardinal Health is recalling 531 boxes of OneTouch Ultrasoft Lancets shipped February-March 2021 due to temperature exposure during shipment that may cause inaccurate test results.

    Product
    ONETOUCH ULTRASOFT LANCETS 100 COUNT Item Number: 3007788
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21157·2021-06-30

    Children's Nightgowns Recalled for Flammability Standard Violation

    About 4,900 Booph children's nightgowns sold on Amazon from March through June 2021 are being recalled because they fail to meet federal flammability standards for sleepwear, posing a burn risk to children.

    Product
    Children's Nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0638-2021·2021-06-30

    Mephyton Phytonadione 5 mg Tablets Recall for Failed Impurity Specifications

    Bausch Health Companies is recalling Mephyton (Phytonadione) 5 mg tablets nationwide because certain lots failed impurities and degradation specifications. Affected consumers should contact their healthcare provider.

    Product
    Mephyton (Phytonadione) 5 mg tablets, 100-count tablets, Rx Only, Manufactured for: Valeant Pharmaceuticals North America, LLC, Bridgewater, NJ, 08807, USA, NDC 0187-1704-05.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0702-2021·2021-06-30

    Favorite Day Caramel Cashew Trail Mix Recalled for Plastic Contamination

    John B. Sanfilippo & Son Inc. is recalling Favorite Day Caramel Cashew Trail Mix nationwide because the product may contain stringy pieces of flexible plastic.

    Product
    favorite day caramel cashew Trail Mix, Product Number 04312. Milk Chocolate caramel balls, cashews, M&M'S milk chocolate candies and Peanuts. Net Wt 14 oz. (396g), UPC 85239-15671
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1945-2021·2021-06-30

    Medical Action Industries Hemostats Recalled for Flaking Metal Defects

    Medical Action Industries is recalling Mosquito Hemostats due to potential flaking metal and brown spots on the devices. The recall affects 23 boxes of surgical instruments distributed nationwide.

    Product
    Medical Action INDUSTRIES INC., Disposable Instrument Pack Mosquito Hemostat, REF 56220
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1942-2021·2021-06-30

    Blood Glucose Test Strips Recalled for Temperature Exposure During Shipping

    Cardinal Health is recalling ACCU-CHEK SMARTVIEW 100 test strips distributed in Florida, Georgia, and South Carolina due to temperature excursions during shipping that may cause inaccurate glucose readings.

    Product
    ACCU-CHEK SMARTVIEW 100 TEST STRIPS Item Number: 4742862
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0636-2021·2021-06-30

    Diflorasone Diacetate Ointment recalled for foreign particles

    Teligent Pharma is recalling Diflorasone Diacetate Ointment USP 0.05% due to the presence of foreign particles found during routine stability testing. The recall affects 6,240 tubes distributed nationwide.

    Product
    Diflorasone Diacetate Ointment USP, 0.05%, packaged in a)15 g (NDC 52565-063-15) and b) 30 g (NDC 52565-063-30) tubes, Rx only, Manufactured by: Teligent Pharma, Inc, Buena, NJ 08310.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0701-2021·2021-06-30

    Favorite Day Peanut Butter Chocolate Trail Mix Recalled for Plastic Pieces

    John B. Sanfilippo & Son Inc. is recalling Favorite Day Peanut Butter Chocolate Trail Mix because some packages may contain stringy pieces of flexible plastic.

    Product
    favorite day peanut butter chocolate Trail Mix, Product Number 04315. Peanut butter cups, Milk Chocolate-covered cereal squares, peanuts, chocolate chips and Peanut Butter Chips. Net Wt 8 oz. (226g), UPC 85239-15683
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1935-2021·2021-06-30

    Vicks vaporizers recalled for temperature exposure during shipping

    Cardinal Health is recalling Vicks 1.5-gallon vaporizers exposed to temperature excursions during shipping delays in February-March 2021, which may cause inaccurate results. Affected units were distributed in Florida, Georgia, and South Carolina.

    Product
    VAPORIZER VICKS 1.5GAL Item Number: 2354942
    Category
    Medical Device
    Distribution
    Distributed nationwide