The Recall Desk

State

Missouri product recalls

73,817 recalls have nationwide distribution and so reach Missouri. 8,501 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,501
Critical
1,339
Severe
2,204
Most recent
2026-11-04

Of the 8,501 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 2,204 (26%) are Severe.

These figures cover only the 8,501 recalls whose distribution notice names Missouri specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45276–45300 of 82318

  • HighCPSC·18049·2017-11-30

    Synodrin Pain Relieving Cream Recalled for Non-Child-Resistant Packaging

    Natural Solutions for Life is recalling Synodrin Pain Relieving Cream because the jar caps are not child-resistant, posing a poisoning risk to young children.

    Product
    Maximum Strength Synodrin Pain Relieving Cream with Lidocaine
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18050·2017-11-30

    Flos Recalls Pendant Light Fixtures Due to Impact Injury Hazard

    Flos Inc. is recalling specific Romeo Moon and Romeo Louis II pendant light fixtures because the internal glass diffuser can detach and fall, posing an impact injury hazard.

    Product
    Pendant light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0167-2018·2017-11-29

    Zimmer Biomet ROSA Brain 3.0.0 Software Recall for Communication Errors

    Zimmer Biomet is recalling 18 units of ROSA Brain 3.0.0 software due to communication errors between software components and the controller.

    Product
    ROSA Brain 3.0.0 Usage: The device is intended for the spatial positioning and orientation of instrument holders or tool guides to be used by neurosurgeons to guide standard neurosurgical instruments (biopsy needle, stimulation or recording electrode, endoscope). The device…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0072-2018·2017-11-29

    Spacelabs Arkon Anesthesia Workstation Recalled for Mechanical and Display Failures

    Spacelabs Healthcare is recalling 110 Arkon Anesthesia Workstations due to failures in ventilation, gas delivery, and display alarms.

    Product
    Arkon Anesthesia Delivery System, Model 99999, and software version 2.61 and upgrade kit 050-9043-00 Rev G. The Spacelabs Arkon Anesthesia Workstation is intended for use in the hospital environment and operating room. It may be used for the delivery of oxygen, air and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V768000·2017-11-29

    Ford Recalls 2017 F-53 and F-59 Chassis for Brake Fluid Leak Risk

    Ford is recalling 2017 F-53 and F-59 chassis because missing plugs in the brake control unit may cause fluid leaks or air ingestion, increasing stopping distance.

    Product
    FORD — FORD F-59, F-53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V766000·2017-11-29

    Volkswagen Recalls 2018 Atlas Vehicles Due to Fuel Tank Leak Risk

    Volkswagen is recalling 2018 Atlas vehicles because the fuel tank may have insufficient wall thickness, potentially causing a fuel leak and increasing fire risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0121-2018·2017-11-29

    Halyard Turbo-Cleaning Closed Suction System Saline Vials Recalled for Leaking Risk

    Halyard Health is recalling specific lots of 15ml saline vials used in the Turbo-Cleaning Closed Suction System because they may leak, potentially exposing contents to infectious agents.

    Product
    Halyard Turbo-Cleaning Closed Suction System for Adults, 14 F, T-Piece, Wet Pak. 12 vials per kit, 20 kits per case.
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Food)·F-0335-2018·2017-11-29

    Shoreline Fruit Recalls Dark Chocolate Covered Cherries for Undeclared Milk

    Shoreline Fruit is voluntarily recalling dark chocolate covered cherry products due to undeclared milk in the dark chocolate coating.

    Product
    Dried Dark Chocolate Covered Cherries, The products are packaged in 25-pound corrugated boxes and 6 oz. and 24 oz. stand-up pouch packaging.
    Category
    Food
    Distribution
    47 states
  • HighFDA (Devices)·Z-0164-2018·2017-11-29

    Medline Transfer/Gait Belt Recall Due to Locking Mechanism Failure

    Medline Industries is recalling 1,428 Transfer/Gait Belts because the locking mechanism may fail to secure the strap, allowing it to slip through the buckle.

    Product
    Transfer/Gait Belt, Plastic, Wipeable, packaged in plastic bag, 36 plastic bags per box.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0114-2018·2017-11-29

    3M Recalls Bair Hugger Temperature Sensors Due to Programming Error

    3M is recalling Bair Hugger temperature sensors because a programming error may cause the device to display a temperature lower than the patient's actual body temperature.

    Product
    3M Bair Hugger(TM) Normothermia System, Temperature Monitoring System Sensors Model 360 (Part Number 36000)
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-0115-2018·2017-11-29

    Zimmer Biomet Recalls ROSA Surgical Device Due to Software Error

    Zimmer Biomet is recalling 64 ROSA Surgical Device 2.5.8 units because a software defect may change tool orientation without user command.

    Product
    ROSA Surgical Device 2.5.8
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0162-2018·2017-11-29

    Medline Recalls Sensicare Green Surgical Gloves Due to Potential Sterility Breach

    Medline Industries is recalling 8,000 units of Sensicare Green Surgical Gloves because a possible open seal on the packaging could compromise sterility.

    Product
    Sensicare Green Surgical Glove, PI, LF, PF. Packaged in a poly/poly peel pouch with Sunoco films, sterile. Surgical glove.
    Category
    Medical Device
    Distribution
    48 states
  • HighFDA (Devices)·Z-0118-2018·2017-11-29

    Halyard Turbo-Cleaning Closed Suction System Recalled for Leaking Saline Vials

    Halyard Health is recalling Turbo-Cleaning Closed Suction Systems because saline vials may leak, potentially exposing contents to infectious agents.

    Product
    Halyard Turbo-Cleaning Closed Suction System for Adults, 14 F, DSE, Wet Pak. 12 saline vials per kit, 20 kits per case.
    Category
    Medical Device
    Distribution
    38 states
  • HighNHTSA·17V767000·2017-11-29

    Ford Recalls 2016 Explorer and F-150 for Seat Bolt Defect

    Ford is recalling 2016 Explorer and F-150 vehicles because loose seat bolts may cause cushions to detach in a crash, increasing injury risk.

    Product
    FORD — FORD EXPLORER, F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0117-2018·2017-11-29

    Halyard Closed Suction System Recalled for Potential Saline Vial Leaking

    Halyard Health is recalling specific lots of Closed Suction Systems because saline vials may leak, potentially exposing contents to infectious agents.

    Product
    Halyard Closed Suction System for Adults with BALLARD Technology WET PAK. 12 saline vials per kit, 20 kits per case.
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Devices)·Z-0125-2018·2017-11-29

    Halyard Health Recalls NOVAPLUS Endotracheal Suction Kits Due to Leaking Vials

    Halyard Health is recalling NOVAPLUS Endotracheal WET PAK Closed Suction Systems because 15ml saline vials may leak, potentially exposing contents to infectious agents.

    Product
    NOVAPLUS* Endotracheal WET PAK* Closed Suction System for Adults with BALLARD* Technology, Double Swivel Elbow, 14 F. 6 vials per kit, 20 kits per case.
    Category
    Medical Device
    Distribution
    38 states
  • HighCPSC·18045·2017-11-29

    Toys R Us Recalls Clay Craft Kits Due to Mold Exposure Risk

    Toys R Us is recalling approximately 6,000 'totally me!' clay craft kits sold at Babies R Us and Toys R Us stores because the clay may contain mold, posing a risk of respiratory or other infections.

    Product
    Clay craft kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0122-2018·2017-11-29

    Halyard Closed Suction System Recalled Due to Saline Vial Leaking Risk

    Halyard Health is recalling specific lots of Closed Suction Systems because 15ml saline vials may leak, potentially exposing contents to infectious agents.

    Product
    Halyard Closed Suction System for Adults, 14 F, T-Piece, Wet Pak. 12 or 6 vials per kit, 20 kits per case.
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Devices)·Z-0124-2018·2017-11-29

    Halyard Closed Suction System Saline Vials Recalled for Leaking Risk

    Halyard Health is recalling specific lots of saline vials used in closed suction systems because they may leak, potentially exposing the contents to infectious agents.

    Product
    Halyard Closed Suction System for Adults, 14 F, T-Piece, MDI, Wet Pak. 12 vials per kit, 20 kits per case.
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Devices)·Z-0123-2018·2017-11-29

    Halyard Turbo-Cleaning Closed Suction System Recalled for Potential Saline Vial Leaking

    Halyard Health is recalling Turbo-Cleaning Closed Suction Systems because 15ml saline vials may leak, potentially exposing contents to infectious agents.

    Product
    Halyard Turbo-Cleaning Closed Suction System for Adults, 14 F, DSE, MDI, Wet Pak. 12 vials per kit, 20 kits per case.
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Devices)·Z-0119-2018·2017-11-29

    Halyard Closed Suction System Saline Vials Recalled for Potential Leaking

    Halyard Health is recalling specific lots of saline vials used in closed suction systems because they may leak, potentially exposing contents to infectious agents.

    Product
    Halyard Closed Suction System for Adults, 14 F, DSE, Wet Pak. 12 or 6 vials per kit, 20 kits per case.
    Category
    Medical Device
    Distribution
    38 states