The Recall Desk

State

Missouri product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35851–35875 of 82241

  • ModerateFDA (Drugs)·D-1822-2019·2019-08-28

    Medtech Recalls Clear Eyes Redness Relief Eye Drops for Quality Control Issues

    Medtech Products, Inc. is recalling Clear Eyes Redness Relief eye drops due to concerns about quality assurance controls at the manufacturing facility.

    Product
    Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%) eye drops, packaged in a) 0.5 FL OZ (15 mL) bottle (UPC 6 78112 25415 6); b) 1 FL OZ (30 mL) bottle (UPC 6 78112 25419 4); c) 0.2 FL OZ (6 mL) bottle, Handy Pocket Pal (UPC 6 78112 25418 7); Distributed…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2335-2019·2019-08-28

    BD Max GC RT PCR Assay Recalled for Improperly Sealed Foil Bags

    Becton Dickinson is recalling BD Max GC RT PCR Assay kits because foil bags containing extraction tubes may not be sealed properly.

    Product
    Kit BD Max GC RT PCR Assay; Catalog # 443486
    Category
    Medical Device
    Distribution
    38 states
  • ModerateFDA (Devices)·Z-2321-2019·2019-08-28

    BD Max Check-Points CPO IVD Kit Recalled for Improperly Sealed Foil Bags

    Becton Dickinson is recalling 130 units of BD Max Check-Points CPO IVD kits because foil bags containing extraction tubes may not be sealed properly.

    Product
    Kit BD Max Check-Points CPO IVD EU; Catalog # 278102
    Category
    Medical Device
    Distribution
    38 states
  • ModerateFDA (Drugs)·D-1824-2019·2019-08-28

    Medtech Recalls Clear Eyes Maximum Itchy Eye Relief Drops

    Medtech Products is recalling Clear Eyes Maximum Itchy Eye Relief drops due to quality assurance concerns at the manufacturing facility.

    Product
    Clear eyes MAXIMUM ITCHY EYE RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%, Zinc Sulfate 0.25%) eye drops, 0.5 FL OZ (15 mL) bottle, Distributed by Medtech Products Inc., Tarrytown, NY 10591, A Prestige Brands Company, UPC 6 78112 65920 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1826-2019·2019-08-28

    Medtech Recalls Clear Eyes Assorted Displays Due to Quality Control Concerns

    Medtech Products is recalling Clear Eyes Assorted IRC Displays due to concerns about quality assurance controls in the manufacturing facility.

    Product
    Clear Eyes Assorted IRC Display; each display contains 6 each of a) Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.12%) eye drops, 0.5 FL OZ (15 mL) bottle (UPC 6 78112 25415 6); b) Clear eyes MAXIMUM REDNESS RELIEF (Glycerin 0.5%, Naphazoline…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2354-2019·2019-08-28

    Molded Products Recalls Mislabelled Luer Lock Sets for IV Administration

    Molded Products Inc is recalling 130,000 Luer Lock Sets (Catalog # MPC-125) because some packages were incorrectly labeled as a different product.

    Product
    Luer Lock Set - Catalog # MPC-125, for IV administration sets.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2351-2019·2019-08-28

    Siemens ACUSON NX2 Ultrasound Systems Recalled for Acoustic Output Defect

    Siemens is recalling 70 ACUSON NX2 ultrasound systems because internal testing found transducers may exceed defined acoustic output power values.

    Product
    ACUSON NX2 Elite Diagnostic Ultrasound System, Model # 11284500, RX Only, Siemens Medical Solutions, containing software version VA10A, VA10B, VA11A, VA11B; UDI # 04056869050775 The ACUSON NX2 diagnostic ultrasound imaging systems are intended for the following applications…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2325-2019·2019-08-28

    BD Max ExK DNA 2 USA Extraction Tube Sealing Defect Recall

    Becton Dickinson is recalling BD Max ExK DNA 2 USA kits because foil bags containing extraction tubes may not have been sealed properly.

    Product
    Kit BD Max ExK DNA 2 USA; Catalog # 442819
    Category
    Medical Device
    Distribution
    38 states
  • LowFDA (Devices)·Z-2291-2019·2019-08-28

    FDA Recalls MICRO-TEMP LT Heat Therapy Systems Due to Tissue Damage Risk

    Cincinnati Sub-Zero is recalling 2,079 MICRO-TEMP LT heat therapy systems because updated warnings indicate that exceeding 40°C for extended periods may cause tissue damage.

    Product
    MICRO-TEMP LT System, Model 749- Localized Heat Therapy System is intended to warm a patient's body part through conductive heat transfer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E059000·2019-08-27

    Chrysler Recalls Mopar Rear Step Kits for 2019 Ram 1500 Trucks

    Chrysler is recalling Mopar Rear Step Kits for 2019 Ram 1500 trucks because they may contact the fuel tank in a rear crash, causing a leak and fire risk.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19188·2019-08-27

    Happy Plugs Recalls Wireless Headphones Due to Burn Hazard

    Happy Plugs is recalling Bluetooth Wireless II headphones because the included micro-USB charging cable can cause overheating and burns. No injuries have been reported.

    Product
    Happy Plugs Bluetooth Wireless II Headphones
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·19773·2019-08-26

    BRP Recalls 2019 Ski-Doo Snowmobiles Due to Fuel Leak Fire Hazard

    BRP is recalling about 2,900 2019 Ski-Doo snowmobiles with 850 E-TEC engines because a fuel leak at the injector poses a fire hazard. Consumers should stop using the vehicles and contact a dealer for a free repair.

    Product
    2019 Ski-Doo snowmobiles equipped with an 850 E-TEC engine
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E057000·2019-08-26

    MAC Tools tire pressure gauges recalled due to inaccurate pressure readings

    Stanley Assembly Technologies is recalling certain MAC Tools tire pressure gauges because they may display lower than actual pressure when battery voltage is low, potentially causing tires to burst.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V623000·2019-08-26

    Lance Camper Recalls 2018-2019 855S Trailers Due to Fire Risk

    Lance Camper is recalling 2018-2019 855S trailers because a wire may contact the refrigerator burner box, increasing fire risk.

    Product
    LANCE CAMPER — LANCE CAMPER LANCE CAMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V615000·2019-08-22

    Volkswagen Recalls Vehicles Due to Ignition Key Removal Risk

    Volkswagen is recalling 679,027 vehicles because silicate buildup may allow the key to be removed when the transmission is not in Park, increasing the risk of a rollaway.

    Product
    VOLKSWAGEN — VOLKSWAGEN BEETLE, GOLF SPORTWAGEN, JETTA, GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E056000·2019-08-22

    ZF Brake Calipers Recalled for Incorrect Assembly Fluid and Drag Risk

    ZF North America is recalling brake calipers that may contain incorrect assembly fluid, causing seals to swell and brakes to drag.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:DISC:CALIPER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V618000·2019-08-22

    Peterbilt 337 and 348 Trucks Recalled for Steering Column Defect

    PACCAR is recalling 2019-2020 Peterbilt 337 and 348 trucks because a steering shaft weld may crack, causing loss of steering control.

    Product
    PETERBILT — PETERBILT 348, 337
    Category
    Vehicle
    Distribution
    Distributed nationwide