The Recall Desk

State

Missouri product recalls

73,213 recalls have nationwide distribution and so reach Missouri. 8,493 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,493
Critical
1,344
Severe
1,882
Most recent
2026-09-23

Of the 8,493 recalls naming Missouri we have scored against our rubric, 1,344 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,882 (22%) are Severe.

These figures cover only the 8,493 recalls whose distribution notice names Missouri specifically. The 73,213 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14901–14925 of 81706

  • HighFDA (Devices)·Z-0216-2024·2023-11-08

    Cepheid Xpert Xpress Strep A test kits may produce invalid results

    Cepheid is recalling 1,413 Xpert Xpress Strep A test kits due to a defect in the included pipettes. Defective pipettes may fail to dispense adequate sample volume, resulting in invalid test results or no test result.

    Product
    Xpert Xpress Strep A, REF:Xprstrepa-CE-10, CE IVD,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0080-2024·2023-11-08

    Opium Tincture recalled for subpotent morphine content nationwide

    Edenbridge Pharmaceuticals recalled opium tincture nationwide because the morphine concentration fell below labeled potency. The voluntary recall affected 4,548 bottles.

    Product
    OPIUM TINCTURE DEODORIZED — OPIUM TINCTURE DEODORIZED (MORPHINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0085-2024·2023-11-08

    Bisoprolol Fumarate and Hydrochlorothiazide Tablets Recalled for Failed Quality Specifications

    Glenmark Pharmaceuticals is recalling Bisoprolol Fumarate and Hydrochlorothiazide Tablets due to failed impurities and degradation specifications. The recall affects 480 bottles distributed nationwide.

    Product
    BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE — BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0212-2024·2023-11-08

    Hillrom Progressa+ Hospital Beds Recalled for Static Electricity Risk

    Hillrom Progressa+ hospital beds (499 units) are being recalled due to potential static electricity buildup that could cause mild shock to operators during transport. The affected units were distributed nationwide.

    Product
    HILLROM PROGRESSA+ BED, Product Codes: P7501A000016, P7501A000019, P7501A000031, P7501A000032, P7501A000033, P7501A000052, P7501A000053, P7501A000054, P7501A000055, P7501A001851, P7501A001972, P7501A001973, and P7501A001974
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0204-2024·2023-11-08

    Coapt ControlSeal Electrode Recalled Due to Burn and Blistering Risk

    Coapt LLC is recalling 109 ControlSeal Electrodes due to risk of minor burns or blistering if exposed to direct sunlight or warm temperatures exceeding 12 hours, or if the battery is damaged.

    Product
    Coapt ControlSeal Electrode, cutaneous EMG Electrode
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0217-2024·2023-11-08

    DBS Lead Device Recall: Use By Date Label Discrepancy

    Medtronic is recalling a small number of LEAD 3387S-40 deep brain stimulation devices due to discrepancies in the Use By Date printed on the outer package versus the individual product label.

    Product
    LEAD 3387S-40 STIMLOC DBS, Model Number 3387S-40. Electrical implantable device.
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0197-2024·2023-11-08

    Quest Medical Recalls Q2 Multiport Intravenous Extension Sets

    Quest Medical is recalling 17,700 Q2 Multiport Extension Sets distributed in the US and Canada. The nature of the defect is not detailed in available source documentation.

    Product
    Q2 Multiport Extension set, REF: 9520, Rx Only Sterile, single use non-pyrogenic intravenous fluid administration sets with a multiport IV manifold and integrated back-check valves, pre-attached needleless injection sites, drip chamber and roller clamps.
    Category
    Medical Device
    Distribution
    19 states
  • ModerateFDA (Devices)·Z-0205-2024·2023-11-08

    Pediatric Tracheostomy Tube Recalled Due to Incorrect Box Expiration Date Label

    Smiths Medical recalls a pediatric tracheostomy tube because the outer box shows an incorrect expiration date (3/17/2021) while the actual product has the correct date (3/17/2026). The discrepancy could cause confusion about product validity.

    Product
    Smiths Medical Portex Bivona Pediatric Tracheostomy Tube, Cuffless, Model 60P045, Sterile.
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Drugs)·D-0082-2024·2023-11-08

    Iodine Solution Recalled for Manufacturing Compliance Deviations

    Safecor Health recalls Strong Iodine Solution nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The prescription product was distributed in multiple lots across the U.S.

    Product
    STRONG IODINE SOLUTION — STRONG IODINE SOLUTION (STRONG IODINE SOLUTION)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V748000·2023-11-07

    Alexis Fire Equipment Recalls Fire Apparatus Due to Parking Brake Defect

    Alexis Fire Equipment is recalling 2021-2024 Fire Apparatus vehicles because a defect in the inversion valve may delay parking brake engagement, increasing the risk of unintentional vehicle movement.

    Product
    ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V746000·2023-11-07

    Mack Recalls 2024 MD Trucks Due to Steering Wheel Bolt Issue

    Mack Trucks is recalling 2024 MD trucks because the steering wheel attachment bolt may loosen and separate, potentially causing the steering wheel to detach.

    Product
    MACK — MACK MD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E086000·2023-11-07

    Cruise Recalls 950 Vehicles for Automated Driving System Software Defect

    Cruise LLC is recalling 950 vehicles because a software defect in the Collision Detection Subsystem may cause the vehicle to move after a crash.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V747000·2023-11-07

    Spartan Fire Emergency Vehicles Recalled for Parking Brake Defect

    Custom Fire Apparatus is recalling 2021-2024 Spartan emergency vehicles because a parking brake defect may allow unintentional movement, increasing crash risk.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, FC-94, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V749000·2023-11-07

    Peterbilt Recalls 2024 520 Trucks Due to Engine Bracket Risk

    PACCAR is recalling 2024 Peterbilt 520 vehicles because a rear lifting bracket may detach, posing an injury risk during engine lifting.

    Product
    PETERBILT — PETERBILT 520
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V744000·2023-11-06

    2024 Buick Envista Software Update: Instrument Panel Display Blanking Issue

    General Motors recalls certain 2024 Buick Envista vehicles for a software defect that may cause the instrument panel display to go blank, preventing visibility of critical safety information like vehicle speed and warning lights.

    Product
    BUICK — BUICK, CHEVROLET ENCORE GX, TRAX, ENVISTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·23C005000·2023-11-06

    Evenflo Titan 65 Child Seat Recalled for Missing Warning Labels

    Evenflo is recalling one Titan 65 child seat because it is missing required warning labels, which may increase the risk of injury to the occupant.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V743000·2023-11-03

    Tesla Model S and Model X Incorrect Air Bag Recall

    Tesla is recalling 2021-2024 Model S and Model X vehicles because an incorrect air bag was installed when the steering wheel was replaced. The incompatible air bag could deploy incorrectly during a crash, increasing the risk of injury.

    Product
    TESLA — TESLA MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V739000·2023-11-03

    Forest River Travel Trailers Electrical Wire Gauge Defect Recall

    Forest River is recalling 2023-2024 Sandstorm, Stealth, and 2024 Shockwave travel trailers. The electrical wire from the 50-amp inlet has incorrect gauge and may melt, creating a fire hazard.

    Product
    FOREST RIVER — FOREST RIVER SANDSTORM, STEALTH, SHOCKWAVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V742000·2023-11-03

    Gulf Stream Recalls 2024 Travel Trailers with Incorrect Tire Certification Labels

    Gulf Stream is recalling 2024 travel trailers because incorrect tire size and pressure information on the Federal certification label may lead to overinflation and loss of vehicle control.

    Product
    GULF STREAM — GULF STREAM FRIENDSHIP, AMERI-LITE, INDEPENDENCE, CONQUEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V737000·2023-11-02

    Freightliner M2 and 114SD Recall for Engine Lifting Bracket Defect

    Daimler Trucks North America is recalling 2024 Freightliner M2 and 114SD vehicles because an engine lifting bracket may detach, posing an injury risk.

    Product
    FREIGHTLINER — FREIGHTLINER M2, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide