The Recall Desk

State

Missouri product recalls

73,737 recalls have nationwide distribution and so reach Missouri. 8,500 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,500
Critical
1,339
Severe
2,203
Most recent
2026-10-28

Of the 8,500 recalls naming Missouri we have scored against our rubric, 1,339 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,203 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,500 recalls whose distribution notice names Missouri specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31326–31350 of 82237

  • HighFDA (Devices)·Z-2467-2020·2020-07-08

    Radiometer ABL80-FLEX Box Label Recall for Barcode Misinterpretation Risk

    Radiometer Medical ApS is recalling ABL80-FLEX box labels because barcode misinterpretation on analyzers may cause patient mix-ups or delayed treatment.

    Product
    ABL80-FLEX-393-839 Box Label, REF 393-839, IVD, CE, UDI: 05700693938394 - Product Usage: It is intended for use in a laboratory environment, near patient or point-of-care setting.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2446-2020·2020-07-08

    LivaNova Recalls Sterile Disposable Connectors Due to Barrier Breach

    LivaNova USA Inc. is recalling specific lots of Sterile Disposable Connectors because internal tests found potential breaches in the sterile barrier.

    Product
    Sterile Disposable Connectors ASY STR CONN 3/16 STRLE 24. REF/ GTIN for Insert Label:050503000/ 00803622123214
    Category
    Medical Device
    Distribution
    44 states
  • HighFDA (Devices)·Z-2441-2020·2020-07-08

    Mediana Attendant Vital Signs Monitor Recalled for Temperature Measurement Failures

    Mediana Co., Ltd. is recalling 180 Attendant Vital Signs Monitors because failures were found in the temperature measurement function while in predict mode.

    Product
    DIRECT SUPPLY Attendant VITAL SIGNS MONITOR, REF AVSM2 - Product Usage: It is vital sign monitor to monitor noninvasive blood pressure (NIBP), functional arterial oxygen saturation (SpO2), pulse rate (PR), temperature (Temp) for adult, pediatric and neonatal patients in all…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2464-2020·2020-07-08

    LivaNova Recalls Vein Irrigation Cannulas Due to Sterile Barrier Breach

    LivaNova is recalling 325 Vein Irrigation Cannulas because internal tests found potential breaches in the sterile barrier, which could compromise sterility.

    Product
    Vein Irrigation Cannula with blunt tip. ASY VIC, STERILE 25/CS REF/ GTIN for Insert Label: VIC/ 00803622133107
    Category
    Medical Device
    Distribution
    44 states
  • ModerateFDA (Devices)·Z-2435-2020·2020-07-08

    Westmed Recalls Neo-Vent Infant T-Piece Resuscitation Circuits Due to Fit Issues

    Westmed, Inc. is recalling Neo-Vent Infant T-Piece Resuscitation Circuits because a mold repair resulted in non-compliant 15mm OD connections that prevent use with compatible infant resuscitators.

    Product
    Neo-Vent Infant T-Piece Resuscitation Circuit With Infant Mask; Circuit for use on compatible Infant Resuscitators. 15mm OD x 10mm ID connector; REF 0420, Qty:10, Length: 60" (1.5cm), Rx Only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2482-2020·2020-07-08

    Ortho VITROS 5600 Software Recall for Parameter Reset Defect

    Ortho Clinical Diagnostics is recalling VITROS 5600 Integrated System software versions 3.3.3 and below because assay parameters may reset to defaults.

    Product
    VITROS 5600 Integrated System Software Versions 3.3.3 and below Product Code: 6802413 Unique Identifier: 10758750002740
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1361-2020·2020-07-08

    Children's Robitussin DM Recalled for Missing Dosing Cup Graduations

    Glaxosmithkline is recalling 132,336 bottles of Children's Robitussin DM because the included dosing cups lack age-specific measurement markings.

    Product
    CHILDRENS ROBITUSSIN HONEY COUGH AND CHEST CONGESTION DM — CHILDRENS ROBITUSSIN HONEY COUGH AND CHEST CONGESTION DM (DEXTROMETHORPHAN HBR, GUAIFENESIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2466-2020·2020-07-08

    ROi CPS LLC Recalls Respirator Crash Cart Kits Due to Labeling Error

    ROi CPS LLC is recalling 200 Respirator Crash Cart Kits because the kits are labeled with an expiration date later than the soonest component to expire.

    Product
    Respirator Crash Cart Kit
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2484-2020·2020-07-08

    Ortho VITROS XT 7600 Software Recall for Parameter Reset Issue

    Ortho Clinical Diagnostics is recalling VITROS XT 7600 Integrated System software versions 3.5.1 and below because MicroWell Qualitative Assay parameters may reset to defaults.

    Product
    VITROS XT 7600 Integrated System Software Versions 3.5.1 and below Product Code:6844461 Unique Identifier: 10758750031610
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1376-2020·2020-07-08

    Flexion Recalls Zilretta Injectable Suspension Due to Temperature Abuse

    Flexion Therapeutics is recalling 792 kits of Zilretta (triamcinolone acetonide) because the product was stored at room temperature for more than six weeks.

    Product
    Zilretta (triamcinolone acetonide extended-release injectable suspension), 32mg per vial, 5mL vials, Single-dose Kits, Rx Only, Manufactured for: Flexion Therapeutics, Inc. 10 Mall Road, Suite 301, Burlington, MA 01803, NDC 70801-003-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2465-2020·2020-07-08

    ROi CPS Recalls Isolation Droplet Bundle Kits Due to Labeling Error

    ROi CPS LLC is recalling 24 Isolation Droplet Bundle Kits because the kits are labeled with an expiration date later than the expiration date of the soonest component.

    Product
    Isolation Droplet Bundle Kit
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2481-2020·2020-07-08

    Ortho VITROS 3600 System Recalled for Assay Parameter Reset Issue

    Ortho Clinical Diagnostics is recalling 27 refurbished VITROS 3600 Immunodiagnostic Systems because assay parameters may reset to defaults, potentially affecting test results.

    Product
    VITROS 3600 Immunodiagnostic System - Refurbished Product Code: 6802914 Unique Identifier: 10758750007103
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1362-2020·2020-07-08

    Children's Dimetapp Cold & Cough Recalled for Missing Dosing Cup Graduations

    Glaxosmithkline is recalling Children's Dimetapp Cold & Cough bottles because the included dosing cups are missing graduation marks for certain age groups.

    Product
    Childrens Dimetapp Cold & Cough, For ages 6 yrs. & over, 8 FL OZ. bottle, (237 mL), Distributed by: Pfizer Madison, NJ 07940, Made in Canada, UPC: 60300312234196, NDC: 0031-2234-19.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2483-2020·2020-07-08

    Ortho VITROS 5600 System Recall for Software Parameter Reset Issue

    Ortho Clinical Diagnostics is recalling 130 refurbished VITROS 5600 Integrated Systems because software modifications to assay parameters may be inadvertently reset to default.

    Product
    VITROS 5600 Integrated System - Refurbished Software Versions 3.3.3 and below Product Code: 6802915 Unique Identifier: 10758750007110
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2434-2020·2020-07-08

    Westmed Recalls Neo-Vent Infant T-Piece Resuscitation Circuits Due to Fit Issues

    Westmed, Inc. is recalling Neo-Vent Infant T-Piece Resuscitation Circuits because a manufacturing error resulted in non-compliant 15mm OD connections, preventing use with compatible infant resuscitators.

    Product
    Neo-Vent Infant T-Piece Resuscitation Circuit;Circuit for use on compatible Infant Resuscitators. 15mm OD x 10mm ID connector; REF 0415, Qty:10, Length: 60" (1.5cm), Rx Only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2480-2020·2020-07-08

    Ortho VITROS 3600 Software Recall for Parameter Reset Issue

    Ortho Clinical Diagnostics is recalling VITROS 3600 Immunodiagnostic System software versions 3.3.3 and below because MicroWell Qualitative Assay parameters may reset to defaults.

    Product
    VITROS 3600 Immunodiagnostic System Software Versions 3.3.3 and below Product Code: 6802783, Unique Identifier: 10758750002979
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2436-2020·2020-07-08

    Westmed Neo-Vent Infant T-Piece Resuscitation Circuit Recall for Non-Compliant Connections

    Westmed is recalling Neo-Vent Infant T-Piece Resuscitation Circuits because a mold repair resulted in non-compliant 15mm OD connections, preventing use with compatible infant resuscitators.

    Product
    Neo-Vent Infant T-Piece Resuscitation Circuit With Neonatal Mask; Circuit for use on compatible Infant Resuscitators. 15mm OD x 10mm ID connector; REF 0421, Qty:10, Length: 60" (1.5cm), Rx Only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V398000·2020-07-07

    Keystone Recalls Fifth-Wheel Trailers Due to Antenna Separation Risk

    Keystone is recalling 2019-2020 fifth-wheel trailers because the television antenna may detach during transit, creating a road hazard.

    Product
    KEYSTONE — KEYSTONE RAPTOR, COUGAR, CARBON, FUZION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E046000·2020-07-07

    Harbor Freight Recalls Pittsburg Automotive 3 Ton Heavy Duty Steel Jack Stands

    Harbor Freight is recalling 118,000 Pittsburg Automotive 3 Ton Heavy Duty Steel Jack Stands because the base seam weld may fail under load, causing the stand to drop suddenly.

    Product
    EQUIPMENT:MECHANICAL:INTEGRATED JACK/LEVELER/STABILIZER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V396000·2020-07-07

    Chrysler and Dodge Vehicles Recalled for Steering Wheel Emblem Hazard

    Chrysler is recalling specific Town and Country, Grand Caravan, and Nitro models because a loose steering wheel emblem could become a projectile during air bag deployment.

    Product
    CHRYSLER — CHRYSLER, DODGE TOWN AND COUNTRY, NITRO, GRAND CARAVAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V395000·2020-07-06

    Mercedes-Benz Recalls AMG Models Due to Electronic Stability Control Software Error

    Mercedes-Benz is recalling 2019-2020 AMG models because incorrect Electronic Stability Program software may cause the system to react inaccurately, increasing the risk of a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLC63 S, AMG GT63S, AMG GT63, AMG C63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V392000·2020-07-02

    Gillig Recalls 2013-2020 Low Floor Buses Due to Steering Defect

    Gillig is recalling 2013-2020 Low Floor buses because a steering component may fail, causing a loss of power assist and increasing crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V391000·2020-07-02

    Airstream Recalls 2020-2021 Motorhomes Due to Suspension Bolt Defect

    Airstream is recalling 2020-2021 Atlas and Interstate motorhomes because suspension bolts may be too long, potentially breaking and affecting vehicle handling.

    Product
    AIRSTREAM — AIRSTREAM INTERSTATE, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide