The Recall Desk

State

Kansas product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46126–46150 of 79639

  • CriticalFDA (Food)·F-2376-2017·2017-06-21

    L.A. Lucky Sweet Basil Seeds Recalled for Salmonella Risk

    L.A. Lucky Import & Export is recalling sweet basil seeds from Vietnam after Salmonella was found in a related shipment.

    Product
    L.A. LUCKY BRAND SWEET BASIL SEEDS: Hot E 2.1 OZ (60 G) BAGS; 100 BAGS PER CASE; Product of Vietnam. Ingredients: Sweet Basil Seeds Serving Size 1.05 oz. (2 servings per container) Distributed by L.A. Lucky Import & Export, Inc., Bell, CA 90201
    Category
    Food
    Distribution
    14 states
  • CriticalFDA (Food)·F-2367-2017·2017-06-21

    Kroger Simple Truth Macadamia Nuts Recalled for Listeria Risk

    The Kroger Co is recalling Simple Truth Dry Roasted Macadamia Nuts due to potential Listeria monocytogenes contamination.

    Product
    Simple truth Dry Roasted Macadamia Nuts SEA SALT 12 oz bag UPC 0 1111 00247 8 DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Drugs)·D-0918-2017·2017-06-21

    Complete Pharmacy Recalls Non-Sterile Human Chorionic Gonadotropin Vials

    Complete Pharmacy and Medical Solutions LLC is recalling 49 vials of Human Chorionic Gonadotropin due to confirmed bacterial contamination.

    Product
    Human Chorionic Gonadotropin, 15,000 IU per vial, lyophilized for injection, Rx only, Complete Pharmacy & Medical Solutions, Miami Lakes, FL 33014
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V390000·2017-06-21

    Aston Martin Recalls 2012 V8 Vantage for Transmission Fluid Leak Risk

    Aston Martin is recalling 2012 V8 Vantage vehicles because a transmission connector may break, causing a fluid leak that could prevent shifting or cause the vehicle to roll away.

    Product
    ASTON MARTIN — ASTON MARTIN V8 VANTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2547-2017·2017-06-21

    Medtronic Recalls Custom Suture Packs Due to Potential Seal Defects

    Medtronic is recalling custom suture packs because an incomplete inner package seal may cause the suture material to degrade prematurely.

    Product
    CUSTOM SUTURE PACK; Item Number: US1540 and US1614
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V391000·2017-06-21

    Aston Martin Recalls V8 Vantage for Transmission Fluid Leak Risk

    Aston Martin is recalling 2011-2014 V8 Vantage vehicles because a broken clutch fluid line connector may cause hydraulic leaks, preventing gear shifting or causing the vehicle to roll away.

    Product
    ASTON MARTIN — ASTON MARTIN V8 VANTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0899-2017·2017-06-21

    Bausch & Lomb Recalls NasalCrom Nasal Spray Due to Potential Microbial Contamination

    Bausch & Lomb is recalling specific lots of NasalCrom nasal spray due to potential microbial contamination in the manufacturing water.

    Product
    NasalCrom (cromolyn sodium) Nasal Spray, USP, 5.2 mg per spray, 200 metered sprays, 0.88 FL OZ (26 mL) metered spray pump bottle, Distributed by: Medtech Products, Inc., Tarrytown, NY 10591, UPC 8 148332 01101 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2347-2017·2017-06-21

    Biomerieux Recalls VITEK 2 Gram Negative Susceptibility Cards Due to Moisture Risk

    Biomerieux Inc is recalling VITEK 2 Gram Negative Susceptibility cards because compromised container integrity may expose the product to moisture, potentially causing antibiotic degradation.

    Product
    VITEK 2 Gram Negative Susceptibility card (AST-GN09), REF 22008, 20 cards per carton.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2510-2017·2017-06-21

    Biomerieux Recalls VITEK 2 Streptococcus Susceptibility Cards Due to Moisture Risk

    Biomerieux Inc is recalling VITEK 2 Streptococcus Susceptibility cards because compromised container integrity may expose the product to moisture, potentially degrading antibiotic potency.

    Product
    VITEK¿ 2 Streptococcus Susceptibility card (AST-ST02), IVD, REF 420915, 20 cards per carton.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2192-2017·2017-06-21

    GE Healthcare Discovery IQ X-ray System Recalled for Scan Timing Issue

    GE Healthcare is recalling Discovery IQ X-ray systems because a software issue may cause scans to start before a prescribed delay completes.

    Product
    GE Healthcare Discovery IQ X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2535-2017·2017-06-21

    Cook Inc. Recalls Pereyra Ligature Carrier 75 Due to Reprocessing Instructions

    Cook Inc. is recalling 29 Pereyra Ligature Carrier 75 devices because their reprocessing instructions do not provide sufficient detail for cleaning, disinfection, and sterilization.

    Product
    Pereyra Ligature Carrier 75
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2193-2017·2017-06-21

    GE Healthcare Discovery ML X-ray System Recalled for Scan Timing Defect

    GE Healthcare is recalling 10,884 Discovery ML X-ray systems because a defect may cause scans to start before a prescribed delay completes.

    Product
    GE Healthcare Discovery Ml X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2326-2017·2017-06-21

    Pentax Video Nasopharyngolaryngoscopes Recalled for Loose Suction Arms

    Pentax of America Inc is recalling 1,701 Video Nasopharyngolaryngoscopes due to loose suction arms. The action documents corrective measures taken in 2010-2011.

    Product
    Video Naso pharyngo Laryngoscopes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2548-2017·2017-06-21

    Medtronic Recalls Pacemaker Angio X3 Due to Potential Seal Defect

    Medtronic is recalling 478,465 units of the Pacemaker Angio X3 because an incomplete seal on the inner package may cause the suture material to degrade prematurely.

    Product
    SCHRITTMACHER ANGIO X3; Item Number: 4045255423347
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2527-2017·2017-06-21

    Biomerieux Recalls VITEK 2 Gram Negative Susceptibility Cards

    Biomerieux is recalling VITEK 2 Gram Negative Susceptibility cards because container integrity issues may expose the product to moisture, potentially degrading antibiotic potency.

    Product
    VITEK¿ 2 Gram Negative Susceptibility card (AST-GN67), IVD, REF 413399, 20 cards per carton.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2409-2017·2017-06-21

    Biomerieux Recalls VITEK 2 Gram Negative Susceptibility Cards Due to Moisture Risk

    Biomerieux Inc is recalling VITEK 2 Gram Negative Susceptibility cards because compromised container integrity may expose the product to moisture, potentially causing antibiotic degradation.

    Product
    VITEK¿ 2 Gram Negative Susceptibility card (AST-N236), REF 413171, 20 cards per carton.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2183-2017·2017-06-21

    GE Healthcare LightSpeed VCT X-ray System Recalled for Scan Timing Defect

    GE Healthcare is recalling 10,884 LightSpeed VCT X-ray systems because a defect may cause scans to start before the prescribed delay completes.

    Product
    GE Healthcare LightSpeed VCT X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2195-2017·2017-06-21

    GE Healthcare Discovery NM/CT 670 CZT X-ray System Recall

    GE Healthcare is recalling Discovery NM/CT 670 CZT X-ray systems because a defect may cause scans to start before the prescribed delay completes.

    Product
    GE Healthcare Discovery NM/CT 670 CZT X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2370-2017·2017-06-21

    Biomerieux Recalls VITEK 2 Gram Negative Susceptibility Cards Due to Moisture Risk

    Biomerieux Inc is recalling VITEK 2 Gram Negative Susceptibility cards because compromised container integrity may expose the product to moisture, leading to antibiotic degradation.

    Product
    VITEK¿ 2 Gram Negative Susceptibility card (AST-XN01), REF 410025, 20 cards per carton.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2492-2017·2017-06-21

    Biomerieux Recalls VITEK 2 Gram Negative Susceptibility Cards

    Biomerieux Inc is recalling VITEK 2 Gram Negative Susceptibility cards because compromised container integrity may expose the product to moisture, potentially causing antibiotic degradation.

    Product
    VITEK¿ 2 Gram Negative Susceptibility card (AST-N328), IVD, REF 418630, 20 cards per carton.
    Category
    Medical Device
    Distribution
    Distributed nationwide