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.

33001–33025 of 79558

  • ModerateFDA (Devices)·Z-0728-2020·2020-01-01

    Cardinal Health Recalls S.M.A.R.T. Stents for Incorrect MRI Labeling

    Cardinal Health is correcting labeling on S.M.A.R.T. Nitinol Stent Systems that incorrectly stated they were 'MRI Safe' instead of 'MRI Conditional'.

    Product
    S.M.A.R.T. Nitinol Stent System and the S.M.A.R.T. Control Nitinol Stent System. The SMART stent system includes a self-expanding stent made of Nitinol (nickel-titanium alloy) material and a 6 French (2.0 mm) or 7 French (2.3 mm) sheathed delivery system. The stent is laser…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0743-2020·2020-01-01

    Axis-Shield Homocysteine Reagent Recalled for Potential Performance Issues

    Axis-Shield Diagnostics is recalling 740 units of Liquid Stable 2-Part Homocysteine Reagent due to potential performance issues detected during routine testing.

    Product
    Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT, Part Number FHRWR100 - Product Usage: The device can assist in the diagnosis and treatment of patients suspected of having hyperhomocysteinemia and homocystinuria. The device is intended for Professional use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0737-2020·2020-01-01

    Diagnostica Stago Recalls STA Unicalibrator Due to Positive Bias

    Diagnostica Stago is recalling 5,498 units of STA Unicalibrator because a positive bias was confirmed when compared to International Standards.

    Product
    STA UNICALIBRATOR (ref. 00675)
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-0740-2020·2020-01-01

    Ortho Clinical Diagnostics Recalls Urine Electrolyte Diluent Due to Instability

    Ortho Clinical Diagnostics is recalling Urine Electrolyte Diluent because the product may become unstable when stored in a 2mL cup for 7 days.

    Product
    Urine Electrolyte Diluent, Product Code: 1112352 - Product Usage: used to dilute urine specimens for analysis of sodium (Na+) and potassium (K+) on VITROS 250/350/5,1 FS/4600 Chemistry Systems and the VITROS 5600/XT 7600 Integrated Systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0729-2020·2020-01-01

    Cordis Precise Nitinol Stent System Labeling Correction for MRI Information

    Cardinal Health is correcting labeling on Cordis Precise Nitinol Stent Systems because the instructions incorrectly stated the device was MRI Safe instead of MRI Conditional.

    Product
    Cordis Precise Nitinol Stent System. The Cordis PRECISE Nitinol Stent System devices are designed to deliver a flexible, self-expanding endoluminal stent to the carotid vasculature via over-the-wire (OTW) 5.5F or 6F sheathed delivery systems. The stent is cut from a solid…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0628-2020·2020-01-01

    Spectrum Laboratory Products Recalls Subpotent Estriol Micronized USP

    Spectrum Laboratory Products is recalling specific lots of Estriol Micronized USP because assay results did not meet specifications.

    Product
    Estriol [(16a, 17B)-Estra-1,3,5(10)-triene-3,16,17-triol; Oestriol] Micronized, USP, CAS 50-27-1, packaged in a) 1 G glass bottles, b) 5 G glass bottles, c) 25 G glass bottles, d) 100 G glass bottles, e) 500 G glass bottles, and f) 1 KG plastic bottles, Rx Only, Spectrum…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0730-2020·2020-01-01

    Cardinal Health Recalls S.M.A.R.T. Stents for Incorrect MRI Labeling

    Cardinal Health is correcting labeling on S.M.A.R.T. stents that incorrectly stated they were MRI Safe. The correct classification is MRI Conditional.

    Product
    Cordis S.M.A.R.T. CONTROL /S.M.A.R.T. Vascular Stent System. The S.M.A.R.T. CONTROL and S.M.A.R.T. Vascular Stent Systems consist of a self-expanding stent made of Nitinol (nickel-titanium alloy) material that is pre-mounted on an over-the-wire delivery system. The stents…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0723-2020·2020-01-01

    Lifelines Neuro Recalls ElectroTek Temporal Sensor Cables for Labeling Errors

    Lifelines Neuro is recalling 12 ElectroTek Temporal Sensor Cables due to potential incorrect placement labels that could lead to improper electrode placement during EEG studies.

    Product
    ElectroTek Temporal Sensor Cable Gold - Long Length, Single Length - Product Usage: The electroencephalographic system ElectroTek is intended to acquire, display, and store the electrical activity of a patient s brain obtained by placing electrodes on the patient s scalp. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0722-2020·2020-01-01

    Lifelines Neuro Recalls ElectroTek EEG Sensor Cables Due to Labeling Error

    Lifelines Neuro is recalling eight ElectroTek EEG temporal sensor cables because incorrect placement labels could lead to improper electrode positioning during brain activity studies.

    Product
    ElectroTek Temporal Sensor Cable Gold - Long Length, Graduated - Product Usage: The electroencephalographic system ElectroTek is intended to acquire, display, and store the electrical activity of a patient s brain obtained by placing electrodes on the patient s scalp. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0720-2020·2020-01-01

    Abbott Recalls Mislabeled Radiofrequency Cannulas Due to Manufacturing Error

    Abbott Medical is recalling 470 radiofrequency cannulas that were incorrectly labeled with a 5mm active tip length instead of 10mm.

    Product
    CLASSIC Radiofrequency Cannula - Curved, 10 cm, SMK Compatible Electrode, REF C-1005-S - Product Usage: Disposable Radiofrequency Cannulae are provided in either straight, curved, or curved blunt geometries with a stylet inserted in the cannula. Cannulae are insulated except for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0739-2020·2020-01-01

    Ortho Clinical Diagnostics Recalls VITROS 7% BSA Diluent Due to Instability

    Ortho Clinical Diagnostics is recalling VITROS 7% BSA diluent because it may become unstable when stored in a 2mL cup for seven days.

    Product
    7% BSA (Bovine Serum Albumin), Product Code: 8262487 - Product Usage: is used to dilute samples when assay values exceed the reportable (dynamic) range using the VITROS 250/350/5,1 FS/4600 Chemistry Systems and VITROS 5600/XT 7600 Integrated Systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0742-2020·2020-01-01

    Axis-Shield Homocysteine Reagent Recalled for Potential Performance Issues

    Axis-Shield Diagnostics is recalling 740 units of Liquid Stable 2-Part Homocysteine Reagent due to potential under-recovery of sample results.

    Product
    Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT, Part Number FHBC100 - Product Usage: The device can assist in the diagnosis and treatment of patients suspected of having hyperhomocysteinemia and homocystinuria. The device is intended for Professional use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0626-2020·2020-01-01

    Pharmedium Recalls Subpotent Repinephrine Bitartrate Injection Bags Nationwide

    Pharmedium Services LLC is voluntarily recalling 864 bags of repinephrine bitartrate injection because the drug was subpotent. The recall covers nationwide distribution in the U.S.

    Product
    NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Injection USP (16 mcg per mL) Total Volume 508.00 mL Viaflex Bag, High Alert, Rx Only, PharMEDium Services LLC., 12620 W Airport Blvd #130 Sugar Land, TX 77478.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0745-2020·2020-01-01

    Tosoh AIA-PACK B12 Pretreatment Set Recalled for Barcode Reading Errors

    Tosoh Smd Inc is recalling AIA-PACK B12 Pretreatment Sets due to barcode scanning issues that may delay diagnostic results.

    Product
    AIA-PACK B12 Pretreatment Set- IVD for diagnostic use for pre-treatment of calibrators/controls. Part Number: 020706
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0627-2020·2020-01-01

    Pharmedium Recalls Subpotent Repinephrine Bitartrate Injection Bags

    Pharmedium Services LLC is recalling 5,808 bags of Repinephrine Bitartrate Injection due to subpotent drug levels. The FDA classified this as a Class III recall.

    Product
    NORepinephrine Bitartrate 4 mg added to 250 mL 5% Dextrose Injection USP (16 mcg per mL) Total Volume 254.00 mL Viaflex Bag, High Alert, Rx Only, PharMEDium Services LLC., 12620 W Airport Blvd #130 Sugar Land, TX 77478.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0625-2020·2020-01-01

    Pharmedium Recalls Subpotent Repinephrine Bitartrate Injection Bags

    Pharmedium Services LLC is voluntarily recalling 5,820 bags of subpotent repinephrine bitartrate injection. The FDA classified this as a Class III recall.

    Product
    NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose Injection USP (32 mcg per mL) Total Volume 258.00 mL Viaflex Bag, High Alert, Rx Only, PharMEDium Services LLC., 12620 W Airport Blvd #130 Sugar Land, TX 77478.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V925000·2019-12-30

    Toyne Recalls 2018-2019 Spartan Metro Star and Gladiator Chassis

    Toyne Inc. is recalling 2018-2019 Spartan Metro Star and Gladiator chassis due to a brake relay valve defect that may increase stopping distance.

    Product
    SPARTAN — SPARTAN METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V924000·2019-12-27

    MCI Recalls 2018-2020 Coaches Due to Tag Axle Alignment Risk

    Motor Coach Industries is recalling 2018-2020 D4500 and D4505 coaches because tag axle clamps may slip, causing misalignment and increasing crash risk.

    Product
    MCI — MCI D4500, D4505
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0379-2020·2019-12-25

    Whole Foods Recalls Stir Fry Beef Vegan Due to Listeria Risk

    Whole Foods Market is recalling Stir Fry Beef Vegan served on the hot bar due to possible contamination with Listeria monocytogenes.

    Product
    STIR FRY BEEF VEGAN served on the hot bar
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0352-2020·2019-12-25

    Whole Foods Recalls Vegetable Power Blend for Listeria Risk

    Whole Foods Market is recalling Vegetable Power Blend served on the salad bar due to possible contamination with Listeria monocytogenes.

    Product
    Vegetable Power Blend served on the salad bar
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0403-2020·2019-12-25

    Whole Foods Recalls Korean Chicken Bowls Due to Listeria Risk

    Whole Foods Market is recalling Korean Chicken Bowls due to possible Listeria monocytogenes contamination. The products were sold nationwide from October 10 to November 4, 2019.

    Product
    Bowl, Korean Chicken UPC 26235400000 sold packaged in stores
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0405-2020·2019-12-25

    Whole Foods Recalls Shaved Brussels Sprout Grilled Chicken Bowls

    Whole Foods Market is recalling Shaved Brussels Sprout Grilled Chicken Bowls due to possible Listeria monocytogenes contamination.

    Product
    Bowl, Shaved Brussel Sprout Grilled Chicken UPC 27332900000 sold packaged in stores
    Category
    Food
    Distribution
    Distributed nationwide