The Recall Desk

State

Kansas product recalls

73,809 recalls have nationwide distribution and so reach Kansas. 5,822 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total
5,822
Critical
1,053
Severe
1,486
Most recent
2026-11-04

Of the 5,822 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 1,486 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,822 recalls whose distribution notice names Kansas specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42726–42750 of 79631

  • ModerateFDA (Devices)·Z-0861-2018·2018-03-14

    Bausch & Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades

    Bausch & Lomb is voluntarily recalling specific LaserEdge ophthalmic knives due to an atypical volume of complaints regarding dull blades.

    Product
    LASEREDGE Knives, CLEAR CORNEAL ANGLED 2.75 (6/BOX), REF/PRODUCT CODE E7527, STERILE, Rx Only Product Usage: The LaserEdge Knives are intended for ophthalmic surgery. There is no therapeutic use and they are available to surgeons for use in procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0929-2018·2018-03-14

    Euro Diagnostica Recalls DIASTAT ANA ELISA Kits Due to False Positives

    Euro Diagnostica is recalling 1,090 units of DIASTAT ANA ELISA kits because high background levels may cause false positive test results.

    Product
    DIASTAT anti-Nuclear antibody (ANA) / DIASTAT ANA ELISA. Catalog Number: FANA200. Product Usage: The DIASTAT¿ anti-nuclear antibody (ANA) test is a qualitative enzyme-linked immunosorbent assay (ELISA) for the detection of ANAs in human serum or EDTA plasma. It detects ANAs…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0926-2018·2018-03-14

    Abbott i-STAT DE Handheld Module Software Update Recall

    Abbott Point Of Care Inc. is recalling 894 i-STAT DE handheld data processing modules because a software upgrade resets customized settings and prevents certain data from updating.

    Product
    i-STAT DE handheld data processing module for clinical use, Software Version 2.8, List Number:08K46-01115200 (UDI: 00054749001255)
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-0890-2018·2018-03-14

    Bausch & Lomb Recalls LaserEdge Knives Due to Dull Blade Complaints

    Bausch & Lomb is voluntarily recalling 1,236,749 LaserEdge Knives intended for ophthalmic surgery due to an atypical volume of complaints regarding dull blades.

    Product
    LASEREDGE Knives, 1.6MM X 1.8MM TRAPEZOID ANGLED (6/BOX), REF/PRODUCT CODE E7600, STERILE, Rx Only Product Usage: The LaserEdge Knives are intended for ophthalmic surgery. There is no therapeutic use and they are available to surgeons for use in procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0874-2018·2018-03-14

    Bausch + Lomb Recalls LaserEdge Knives Due to Dull Blades

    Bausch + Lomb is voluntarily recalling 1,236,749 LaserEdge Knives intended for ophthalmic surgery due to an atypical volume of complaints regarding dull blades.

    Product
    LASEREDGE Knives, 2.65MM SLIT KNIFE ANGLED DOUBLE BEVEL GUARDED (6/BOX), REF/PRODUCT CODE E7551ADBG, STERILE, Rx Only Product Usage: The LaserEdge Knives are intended for ophthalmic surgery. There is no therapeutic use and they are available to surgeons for use in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0576-2018·2018-03-14

    Hospira Recalls Labetalol Hydrochloride Injection Due to Cracked Glass Vials

    Hospira Inc. is recalling Labetalol Hydrochloride Injection vials because of cracked glass at the rim, which is covered by the stopper and crimp seal.

    Product
    LABETALOL HYDROCHLORIDE — LABETALOL HYDROCHLORIDE (LABETALOL HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0866-2018·2018-03-14

    Bausch + Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades

    Bausch + Lomb is voluntarily recalling specific LaserEdge ophthalmic knives because an atypical volume of complaints reported dull blades.

    Product
    LASEREDGE Knives, 30 DEGREE STAB BLADE TIP (6/BOX), REF/PRODUCT CODE E7530T, STERILE, Rx Only Product Usage: The LaserEdge Knives are intended for ophthalmic surgery. There is no therapeutic use and they are available to surgeons for use in procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0891-2018·2018-03-14

    Bausch & Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades

    Bausch & Lomb is voluntarily recalling specific LaserEdge ophthalmic knives because of an atypical volume of complaints regarding dull blades.

    Product
    LASEREDGE Knives, 2.0MMX2.2MM TRAPEZOID ANGLED (6/BOX), REF/PRODUCT CODE E7601, STERILE, Rx Only Product Usage: The LaserEdge Knives are intended for ophthalmic surgery. There is no therapeutic use and they are available to surgeons for use in procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0915-2018·2018-03-14

    Ortho-Clinical VITROS DAT Performance Verifier V Recall for Storage Labeling Issues

    Ortho-Clinical Diagnostics is recalling VITROS DAT Performance Verifier V units due to storage labeling errors that may cause lower than expected VITROS BENZ results.

    Product
    VITROS Chemistry Products DAT Performance Verifier V in vitro diagnostic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0889-2018·2018-03-14

    Bausch & Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades

    Bausch & Lomb is voluntarily recalling 1,236,749 LaserEdge Knives used in ophthalmic surgery because of an atypical volume of complaints regarding dull blades.

    Product
    LASEREDGE Knives, 0.88MM ARROW KNIFE ANGLED (6/BOX), REF/PRODUCT CODE E7593, STERILE, Rx Only Product Usage: The LaserEdge Knives are intended for ophthalmic surgery. There is no therapeutic use and they are available to surgeons for use in procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0895-2018·2018-03-14

    Instrumentation Laboratory Recalls Hemosll ReadiPlasTin Kits Due to Performance Issues

    Instrumentation Laboratory is recalling 14,894 Hemosll ReadiPlasTin kits due to reported performance issues, including increased imprecision and out-of-range quality controls.

    Product
    Hemosll ReadiPlasTin (20 ml Size), Part Number 0020301400
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0577-2018·2018-03-14

    Akorn Recalls Atropine Sulfate Ophthalmic Solution Due to Viscosity Failure

    Akorn, Inc. is recalling 31,812 bottles of Atropine Sulfate Ophthalmic 1% Solution because testing revealed low viscosity results.

    Product
    Atropine Sulfate Ophthalmic 1% Solution, USP, 5mL per bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-215-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0585-2018·2018-03-14

    AstraZeneca Recalls Lynparza Capsules Due to Quality Attribute Deviation

    AstraZeneca is recalling 18,056 bottles of Lynparza (olaparib) capsules 50 mg due to elevated levels of a specific quality attribute.

    Product
    Lynparza (olaparib) capsules 50 mg, 112 count bottles, Rx only, Manufactured for: Astra Zeneca Pharmaceuticals LP Wilmington, DE 19850 by: Patheon Pharmaceuticals, Inc. Cincinnati OH 45237 Product of Switzerland NDC 0310-0657-58
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·18120·2018-03-13

    MAAX Spas Recalls Hot Tubs and Swim Spas Due to Fire Hazard

    MAAX Spas is recalling about 550 hot tubs and swim spas in the U.S. because the internal UV generator can ignite, posing a fire hazard.

    Product
    Maax Spas hot tubs and swim spas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18121·2018-03-13

    SwissStop Bicycle Disc Brake Pads Recalled Due to Fall Hazard

    Helvetia Sports is recalling SwissStop EXOTherm cycling disc brake pads because they can separate from the backplate, posing a fall hazard to users.

    Product
    SwissStop EXOTherm cycling disc brake pads
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V169000·2018-03-12

    Ford Recalls Focus and Fusion Vehicles for Clutch Fracture Risk

    Ford is recalling 2013-2016 Focus and Fusion vehicles with manual transmissions because the clutch may fracture, causing transmission damage and fluid leaks that could lead to fire.

    Product
    FORD — FORD FOCUS, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V163000·2018-03-12

    Freightliner Custom Chassis Recalls 2011-2017 RV Chassis for Fire Risk

    Daimler Trucks North America is recalling 9,480 Freightliner Custom Chassis vehicles due to a power steering hose defect that may cause electrical arcing and fire.

    Product
    FCCC — FCCC XCM, XBR, XCL, XCR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V167000·2018-03-12

    Ford Recalls 2014-2018 Fusion and Lincoln MKZ for Steering Wheel Defect

    Ford is recalling 2014-2018 Fusion and Lincoln MKZ vehicles because the steering wheel bolt may loosen, allowing the wheel to detach and causing loss of control.

    Product
    FORD — FORD, LINCOLN FUSION, MKZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E015000·2018-03-09

    SynTec Recalls S3B School Bus Seats Due to Bracket Crack Risk

    SynTec Seating Solutions is recalling S3B Non-Restraint Wall Mounted Seats because the mounting bracket may crack, increasing injury risk in a crash.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V162000·2018-03-09

    Forest River Recalls 2018 Stealth Evo Trailers for Incorrect Tire Placards

    Forest River is recalling 2018 Stealth Evo recreational trailers because the federal placard lists incorrect tire sizes. This error could lead owners to install wrong replacement tires, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER STEALTH EVO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V164000·2018-03-09

    Ferrari Recalls 2016 488 GTB and Spider for Brake Warning Software Error

    Ferrari is recalling 2016 488 GTB and 488 Spider vehicles because a software error may prevent drivers from receiving warnings about critically worn brake discs.

    Product
    FERRARI — FERRARI 488 SPIDER, 488 GTB
    Category
    Vehicle
    Distribution
    Distributed nationwide