The Recall Desk

State

Missouri product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50501–50525 of 82328

  • ModerateFDA (Devices)·Z-0821-2017·2016-12-28

    Stanmore Implants Recalls Tibial Components Due to Packaging Puncture

    Stanmore Implants Worldwide Ltd. is recalling 51 tibial components because the device stem may have punctured the sterile packaging.

    Product
    Tibial Component Metal Cased Small Long; Tibial Component Metal Cased Small Short; Tibial Component Metal Cased Std Long; Tibial Component Metal Cased Std Short The product is a component is a systems that is intended for the replacement if diseased or deficient bone around the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0382-2017·2016-12-28

    Teleflex Medical Recalls Flexi Nozzle Long Sprayers for Inadequate Atomization

    Teleflex Medical is recalling Flexi Nozzle Long sprayers because they may produce a straight stream instead of an atomized plume, potentially causing inadequate anesthesia.

    Product
    FLEXI NOZZLE LONG, 10 Boxes of 25 units each Product Usage: These products are used for the delivery of topical anesthesia via an atomized spray to the oral, nasal, pharyngeal or laryngeal mucosa. Teleflex Medical is recalling these products as they may produce a straight…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0883-2017·2016-12-28

    Amendia Savannah-T Straight Rods Recalled for Packaging Seal Defects

    Amendia, Inc. is recalling Savannah-T Straight Rods because some packages have unacceptable seals with compromised integrity.

    Product
    Savannah-T Straight Rod, 200mm, Part Number 10704-200; Savannah-T Straight Rod, 250mm, Part Number 10704-250; Savannah T-Straight Rod 300mm, Part Number 10704-300; Savannah-T Straight Rod, 400mm, Part Number 10704-400; Savannah-T Straight Rod, 500mm; Savannah-T High Top Straight…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0874-2017·2016-12-28

    Stryker Recalls Sterile Minimally Invasive Surgery Burs Due to Corrosion

    Stryker is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because they may exhibit signs of corrosion.

    Product
    8450-009-040 4.0MM Precision Round, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offering, is used to remove osseous material during surgical cases. Each cutting accessory consists of: " A shank (B) with a notch (A), that fits in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0867-2017·2016-12-28

    Synthes VA Implant Rack Recalled for Incorrect Assembly

    Synthes (USA) Products LLC is recalling 31 units of the VA Implant Rack for the Compact Distal Radius System because incorrect assembly could cause screws to touch the surface beneath the rack.

    Product
    Synthes VA Implant Rack for the Compact Distal Radius System Tray/Surgical/Instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0864-2017·2016-12-28

    Ortho-Clinical Diagnostics Recalls VITROS CRP Slides Due to Result Bias

    Ortho-Clinical Diagnostics is recalling VITROS CRP Slides because the diluent contains endogenous CRP, which can cause falsely high test results if not subtracted.

    Product
    VITROS CRP Slides: 1) VITROS¿ Chemistry Products CRP Slides (250 slides per sales unit), Catalog # 1926740 and 2) , VITROS¿ Chemistry Products CRP Slides (90 slides per sales unit), Catalog # 1926740
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0879-2017·2016-12-28

    OrthoPediatrics PediNail Cortical Screw Recalled for Dimensional Discrepancy

    OrthoPediatrics is recalling 22 PediNail Intramedullary Nailing System 4.5mm X 48mm Cortical Screws because they measure 50mm instead of the labeled 48mm.

    Product
    OrthoPediatrics PediNail Intramedullary Nailing System 4.5mm X 48mm Cortical Screw
    Category
    Medical Device
    Distribution
    7 states
  • LowFDA (Drugs)·D-0225-2017·2016-12-28

    Tom's of Maine Antiperspirant Recalled for Incorrect Back Label

    Les Emballages Knowlton Inc. is recalling Tom's of Maine Naturally Dry Natural Powder Antiperspirant Stick because an incorrect back label was applied to the product.

    Product
    Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick, Distributed by: Tom's of Maine, Kennebunk, ME 04043, Made in Canada, Unit UPC: 077326831953 Case UPC: 10077326831950
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0881-2017·2016-12-28

    Amendia Recalls K-Wires Due to Unacceptable Packaging Seals

    Amendia, Inc. is recalling 5,833 units of K-Wires because the packaging seals are unacceptable, with some showing compromised integrity due to channels or voids.

    Product
    K-Wire 1.4mm x 12in Non-Threaded, Part Number 9080-12U; K-Wire Threaded 1.4mm x 18, Part Number 9080-18T; K-Wire Non-Threaded 1.4mm x 18, Part Number 9080-18U; 1.4mm x 24 Threaded Guide Wire, Part Number 9080-24T; K-Wire Non-Threaded 24, Part Number 9080-24U; Blunt K-Wire, 18…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V952000·2016-12-27

    Southwest Trailer-Mounted Generators Recalled for Tongue Separation Risk

    Southwest is recalling 2013-2016 QP25, QP35, and QP45/50 trailer-mounted generators because the trailer tongue may separate, creating a road hazard.

    Product
    SOUTHWEST — SOUTHWEST QP25 GENERATOR, QP35 GENERATOR, QP45/50 GENERATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V935000·2016-12-27

    Mercedes-Benz Metris Recall: Passenger Air Bag May Not Vent Properly

    Daimler Vans USA is recalling 2017 Mercedes-Benz Metris vans because the front passenger air bag may not vent properly in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V932000·2016-12-27

    Honda Recalls 2016 Odyssey for Second Row Seat Slide Defect

    Honda is recalling 2016 Odyssey vehicles because the second row center seat may slide unexpectedly. This defect increases the risk of injury in a crash.

    Product
    HONDA — HONDA ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V933000·2016-12-27

    Honda Recalls 2011-2016 Odyssey Vehicles Due to Second Row Seat Defect

    Honda is recalling 2011-2016 Odyssey vehicles because the second row outboard seat release lever may remain unlocked, allowing the seat to move unexpectedly during a crash.

    Product
    HONDA — HONDA ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V934000·2016-12-27

    HME Type-6 Wildland Trucks Recalled for Incorrect Weight Rating Label

    HME is recalling 2015-2016 Type-6 Wildland trucks because the certification label may list an incorrect Gross Vehicle Weight Rating, potentially leading to vehicle overload.

    Product
    HME — HME TYPE-6 WILDLAND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·121-2016·2016-12-23

    Gold Medal Packing Recalls Veal Products Due To E. Coli Contamination

    Gold Medal Packing is recalling approximately 4,607 pounds of boneless veal products due to possible E. coli O26 and O45 contamination. No illnesses have been reported.

    Product
    Copper City Meats, DBA Gold Medal Packing — Gold Medal Packing Inc. Recalls Veal Products Due To Possible E. Coli O26 and O45 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V949000·2016-12-23

    DRV Recalls 2016-2017 Elite and Mobile Suites Due to Brake Bolt Issue

    DRV Suites is recalling 2016-2017 Elite and Mobile Suites fifth wheel trailers because brake caliper bolts may loosen, potentially causing a loss of braking capability.

    Product
    DRV — DRV ELITE SUITES ALL, MOBILE SUITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V929000·2016-12-23

    Mack Trucks Recalls Front Wheel Hubs on Pinnacle, Granite, and Titan Models

    Mack is recalling certain 2012-2017 trucks because front wheel hubs may fail, potentially causing loss of vehicle control or dropped parts.

    Product
    MACK — MACK PINNACLE (CXU), GRANITE (GU), PINNACLE (CHU), TITAN (TD)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V930000·2016-12-23

    KME Recalls Fire Trucks Due to Ladder Position Sensor Defect

    Kovatch Mobile Equipment Corp. is recalling certain KME fire trucks because water may leak into the ladder position sensor, increasing the risk of injury.

    Product
    KME — KME PREDATOR SS AERIAL, PREDATOR AERIAL, PREDATOR PANTHER AERIAL, PREDATOR TDA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V950000·2016-12-23

    ARBOC Spirit of Liberty Buses Recalled for Parking Brake Defect

    ARBOC is recalling 2015-2016 Spirit of Liberty transit buses because the parking brake may engage unexpectedly while driving, increasing crash risk.

    Product
    ARBOC — ARBOC SPIRIT OF LIBERTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V923000·2016-12-22

    Pierce Recalls 2015-2016 Dash CF Emergency Vehicles Due to Fire Risk

    Pierce Manufacturing is recalling 2015-2016 Dash CF emergency vehicles because a defective bracket may damage the starter motor, increasing the risk of a fire.

    Product
    PIERCE — PIERCE DASH CF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V925000·2016-12-22

    Ford Recalls 2016-2017 Vehicles for Turbocharger Oil Leak Fire Risk

    Ford is recalling specific 2016-2017 Taurus, Flex, MKT, and Explorer vehicles because improperly brazed turbocharger tubes may leak oil, increasing fire risk.

    Product
    FORD — FORD, LINCOLN FLEX, TAURUS, MKT, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V926000·2016-12-22

    KME Predator Aerial Vehicles Recalled for Brake Defect

    KME is recalling certain Predator SS Aerial and Predator Aerial vehicles because rear brakes may engage without the pedal being pressed, increasing crash and fire risk.

    Product
    KME — KME PREDATOR SS AERIAL, PREDATOR AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide