The Recall Desk

State

Missouri product recalls

73,806 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.

Which agencies issued them

These figures cover only the 8,501 recalls whose distribution notice names Missouri specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39601–39625 of 82307

  • SevereFDA (Drugs)·D-0303-2019·2018-12-19

    Teva Recalls Amlodipine and Valsartan Tablets Due to NDEA Impurity

    Teva Pharmaceuticals USA is recalling Amlodipine and Valsartan Tablets 5 mg/160 mg because FDA testing confirmed the presence of the impurity N-nitrosodimethylamine (NDEA).

    Product
    Amlodipine and Valsartan Tablets 5 mg/160 mg, (a) 30-count bottles (NDC 0093-7690-56) & 90-count bottles (NDC 0093-7690-98), RX Only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD. Jerusalem, 9777402, Israel, Manufactured For: TEVA PHARMACEUTICALS USA, INC. North…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V913000·2018-12-19

    Daimler Trucks Recalls Freightliner and Western Star Models for Steering Defect

    Daimler Trucks is recalling 2017-2019 Freightliner and Western Star trucks because loose steering bolts may cause loss of vehicle control.

    Product
    FREIGHTLINER — FREIGHTLINER, FCCC, WESTERN STAR BUSINESS CLASS M2, 108SD, S2G, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0302-2019·2018-12-19

    Westminster Irbesartan Tablets Recalled Due to NDEA Impurity Traces

    Westminster Pharmaceuticals is recalling specific lots of Irbesartan Tablets because FDA testing found traces of NDEA impurity.

    Product
    Westminster Irbesartan Tablets, USP 300 mg Rx Only Manufactured by: ScieGen Pharmaceuticals, Inc. Hauppauge, NY 11788 Manufactured for: Westminster Pharmaceuticals, LLC. Olive Branch, MS 38654 a) 30 count bottle NDC 69367-121-01; b) 90 count bottle NDC 69367-121-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·18V905000·2018-12-19

    Mercedes-Benz Recalls 2018-2019 GLC63 Models for Air Bag Delay

    Mercedes-Benz is recalling 2018-2019 GLC63 and GLC63S vehicles because the frontal air bag may deploy late for unbelted passengers, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLC63S, AMG GLC63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V904000·2018-12-19

    Volkswagen Recalls Atlas, Jetta, and Golf for Rear Spring Fracture Risk

    Volkswagen is recalling 2018-2019 Atlas, 2015 Golf SportWagen, and 2019 Jetta vehicles because rear coil springs may fracture, potentially causing loss of control.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, JETTA, GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V910000·2018-12-19

    Mercedes-Benz Recalls S-Class Vehicles for Steering Assist Malfunction

    Mercedes-Benz is recalling 2018-2019 S-Class vehicles because the hands-off detection system may fail, keeping steering assist active without driver input.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG S63, S 450, S560
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0713-2019·2018-12-19

    Feast Mode Garlic Beer Seasoning Recalled for Gluten Free Mislabeling

    Feast Mode Blending & Filling is recalling 5,000 units of Garlic Beer Seasoning because the product is mislabeled as 'Gluten Free'.

    Product
    Feast Mode Flavors Garlic Beer Seasoning, Nt. Wt. 5 oz, plastic bottles
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·18V918000·2018-12-19

    BMW Recalls 2019 X5 Models for Missing Air Bag Warning Labels

    BMW is recalling 2019 X5 xDrive40i and xDrive50i vehicles because the sun visors may lack required air bag warning labels, increasing injury risk in crashes.

    Product
    BMW — BMW X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0598-2019·2018-12-19

    Neotract Recalls UroLift System Due to Capsular Tab Delivery Failure

    Neotract is recalling UroLift System devices because the capsular tab may fail to deploy, potentially delaying or preventing treatment completion.

    Product
    UroLift System REF Catalog Number: UL400-4 Tray Contents: UroLift System with Handle Release Tool STERILE R CE 0050 Manufactured By: neotract
    Category
    Medical Device
    Distribution
    44 states
  • HighNHTSA·18V912000·2018-12-19

    Mercedes-Benz Recalls 2018-2019 GLA 250 Models for Sunroof Leak

    Mercedes-Benz is recalling 2018-2019 GLA 250 vehicles because sunroof bonding may allow water leaks that could prevent the window air bag from deploying.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0585-2019·2018-12-19

    GE Healthcare Recalls B20i Patient Monitors Due to Network Overload Restart Risk

    GE Healthcare is recalling 6,458 B20i patient monitors worldwide because network configuration issues may cause the devices to restart unexpectedly.

    Product
    B20i Patient Monitor and B20i V2 Patient Monitor. The device is a portable multiparameter unit to be used for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adult, pediatric, and neonatal patients in a hospital environment and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0582-2019·2018-12-19

    Medtronic HeartWare HVAD Battery Charger Recalled for Incorrect Inductors

    Heartware, Inc. is recalling 2,031 HVAD System Battery Charger units because they were manufactured with incorrect inductors. The recall covers units distributed in the US and multiple international countries.

    Product
    Medtronic HeartWare Ventricular Assist HVAD System Battery Charger Model 1600US - Product Usage: The HeartWare Ventricular Assist System (HVAD) is indicated in the United States (US) and European Union (EU) for use as a bridge to cardiac transplantation (BTT) as well as an…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0703-2019·2018-12-19

    Schwan's Sea Salt Caramel Cashew Ice Cream Recalled for Glass Contamination

    Schwan's is recalling Sea Salt Caramel Cashew Ice Cream due to potential glass contamination. Consumers should check production codes and stop using the product.

    Product
    Schwan's Sea Salt Carmel Cashew Ice Cream (#206). Net Wt 56 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0586-2019·2018-12-19

    GE Healthcare Recalls B40i Patient Monitors Due to Network Restart Risk

    GE Healthcare is recalling 6,864 B40i patient monitors worldwide because network configuration issues may cause the devices to restart unexpectedly.

    Product
    B40i Patient Monitor and B40i Patient Monitor V3 The device is a portable multiparameter unit to be used for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adult, pediatric, and neonatal patients in a hospital environment and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0605-2019·2018-12-19

    Howmedica Recalls Tritanium Posterior Lumbar Cage Implants Due to Fracture Risk

    Howmedica Osteonics Corp. is recalling 28,461 Tritanium Posterior Lumbar cage implants because of reports of fractures occurring during or after surgery.

    Product
    Tritanium Posterior Lumbar (PL) cage intervertebral body fusion implant. Intended for an open, less invasive, and minimally invasive PLIF or TLIF surgical procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V895000·2018-12-19

    Dennis Eagle Elite Refuse Trucks Recalled for Reverse Alarm Mute Switch

    Dennis Eagle is recalling 2017-2018 Elite refuse trucks because the reverse alarm mute switch can prevent the vehicle from beeping in reverse, increasing injury risk.

    Product
    DENNIS EAGLE — DENNIS EAGLE ELITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0584-2019·2018-12-19

    GE Healthcare Recalls PROCARE B40 Patient Monitors Due to Network Overload Risk

    GE Healthcare is recalling 33,065 PROCARE B40 patient monitors because network configuration issues may cause the devices to restart unexpectedly.

    Product
    PROCARE B40 Patient Monitor, V1; and B40 Patient Monitor, V2, V2.1, and V3. The PROCARE Monitor B40 is a portable multiparameter unit to be used for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adult, pediatric, and neonatal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0700-2019·2018-12-19

    Imperial Taste Fried Red Onion Recalled for Undeclared Wheat

    Gemini Food Corporation is recalling Imperial Taste Fried Red Onion because an investigation found undeclared wheat in the ingredients.

    Product
    Imperial Taste Fried Red Onion, Cu Hanh Phi; 24 x 8oz. Item #1760, UPC Code: 741861017607; 24 x 12oz. Item #1761, UPC Code: 741861017614; Ingredients: Red Onion, Palm Oil Product of Vietnam Distributed by Gemini Food Corporation, City Of Inductry, CA 91789
    Category
    Food
    Distribution
    34 states
  • HighNHTSA·18V908000·2018-12-19

    Mercedes-Benz Recalls 2018 S-Class Vehicles for Steering Assist Defect

    Mercedes-Benz is recalling 2018 S-Class and AMG S63 vehicles because an incorrect steering boot installation may keep the Active Steering Assist system engaged while the driver's hands are off the wheel.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH S560, S 560 4MATIC, AMG S63, S 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V906000·2018-12-19

    Mercedes-Benz Recalls 2018 C300 Models for Headlight Adjustment Defect

    Mercedes-Benz is recalling 2,364 2018 C300 and C300 4MATIC vehicles because improperly adjusted headlights may reduce driver visibility and increase crash risk.

    Product
    MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ C 300 4MATIC, C 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0701-2019·2018-12-19

    Fried Garlic Recalled for Undeclared Wheat Ingredient

    Gemini Food Corporation is recalling Imperial Taste Fried Garlic due to undeclared wheat. The product is distributed in multiple states.

    Product
    Imperial Taste Fried Garlic, Tu Phi; 24 x 8oz. Item #1763 UPC Code: 741861017638; 24 x 12oz. Item #1762 UPC Code: 741861017621 Ingredient: Garlic, Palm Oil Product of Vietnam Distributed by Gemini Food Corporation, City of Industry, CA
    Category
    Food
    Distribution
    34 states