The Recall Desk

State

Missouri product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43176–43200 of 82310

  • HighFDA (Devices)·Z-1513-2018·2018-05-02

    BioFire FilmArray BCID Panel Recalled for False Positive Proteus Results

    BioFire Diagnostics is recalling the FilmArray BCID Panel because it may produce false positive Proteus results when used with specific BD BACTEC blood culture bottles.

    Product
    FilmArray BCID Panel (Blood Culture Identification Panel), Catalog numbers RFIT-ASY-0126 (30 test kit) and RFIT-ASY-0127 (6 test kit), when used with all lots of BD BACTEC Blood Culture Bottles, Catalog numbers 442020, 442021, 442023, 442192, 442265, 442194, 442022, 442193…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1514-2018·2018-05-02

    Synthes Stem Extractor Recalled Due to Potential Screw Breakage

    Synthes, Inc. is recalling 31 Stem Extractor f/Guide Bar units because the connection screw may break during use.

    Product
    Stem Extractor f/Guide Bar, Part number 03.401.072. Instrumentation for extraction and revision of Epoca shoulder implants.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1131-2018·2018-05-02

    Frozen Parotta Recalled for Undeclared Milk Allergen

    Maharaja Food Importers is recalling frozen Parotta products because the label lists ghee but fails to declare milk, a major allergen.

    Product
    Parotta Family Pack, UPC: 8 70400 00084 5, Frozen; and Small Parotta, UPC: 870400000012, Frozen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1509-2018·2018-05-02

    Stryker T4 Zipper Toga Recall Due to Material Separation Risk

    Stryker is recalling T4 Zipper Toga sterile garments because material layers may separate, creating a risk of exposure to contaminants.

    Product
    T4 Zipper Toga, X-Large; Catalog number: 0400-850-000 Sterile personal protection garment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1527-2018·2018-05-02

    Recall of EEA Hemorrhoid and Prolapse Stapler Sets Due to Welding Defect

    Covidien LLC is recalling EEA Hemorrhoid and Prolapse Stapler Sets because a defective staple guide may cause bleeding or anastomotic leak during surgery.

    Product
    EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM, Product Number HEM3335, GTIN Number 1 - 10884521047518, GTIN Number 2 - 20884521047515 Product Usage: The EEA Hemorrhoid and prolapse stapler set with DST Series Technology (instrument) is designed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1506-2018·2018-05-02

    Stryker T4 Zipper Toga Sterile Garment Recall for Layer Separation

    Stryker is recalling T4 Zipper Toga sterile personal protection garments because material layers may separate, creating a risk of exposure to contaminants.

    Product
    T4 Zipper Toga, (L/XL); Catalog Number: 0400-820-000 Sterile personal protection garment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0717-2018·2018-05-02

    Coastal Meds Recalls Cyanocobalamin Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling 745 vials of Cyanocobalamin Injectable due to the presence of unknown particulate matter.

    Product
    CYANOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1132-2018·2018-05-02

    MMRF Ela Ada Jaggery Recalled for Undeclared Milk Allergen

    Maharaja Food Importers is recalling frozen MMRF Ela Ada Jaggery because the label lists ghee but fails to declare milk, a major allergen.

    Product
    MMRF Ela Ada Jaggery, UPC: 870400000067, Frozen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1508-2018·2018-05-02

    Stryker T4 Zipper Toga Sterile Garments Recalled for Layer Separation

    Stryker is recalling T4 Zipper Toga sterile personal protection garments because material layers may separate, posing a risk of exposure to contaminants.

    Product
    T4 Zipper Toga, Regular; Catalog number: 0400-830-000 Sterile personal protection garment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1470-2018·2018-05-02

    Zimmer Biomet Recalls ZMS Intramedullary Fixation Smooth Guide Wires

    Zimmer Biomet is recalling ZMS Intramedullary Fixation Smooth Guide Wires due to potential failure of the sterile packaging seal.

    Product
    ZMS Intramedullary Fixation Smooth Guide Wire 3.0 mm Diameter, 100 cm Length; Item Number: 47-2237-037-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1501-2018·2018-05-02

    Stryker T4 Pullover Toga Recalled for Potential Material Separation

    Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, posing a risk of exposure to contaminants.

    Product
    T4 Pullover Toga, L/XL; Catalog Number: 0400-720-000 Sterile personal protection garment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·18148·2018-05-02

    Carter's Recalls Children's Cardigan Sets Due to Choking Hazard

    Carter's is recalling 3-piece penguin cardigan sets because the toggle button can detach, posing a choking hazard to young children.

    Product
    3-piece penguin cardigan sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1504-2018·2018-05-02

    Stryker Recalls T4 Pullover Toga Due to Material Separation Risk

    Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, creating a potential risk of exposure to contaminants.

    Product
    T4 Pullover Toga, X-Large; Catalog Number: 0400-770-000 Sterile personal protection garment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0720-2018·2018-05-02

    Coastal Meds Recalls LIPO-B Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling LIPO-B Injectable-30 mL vials due to the presence of unknown particulate matter.

    Product
    LIPO-B Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1502-2018·2018-05-02

    Stryker T4 Pullover Toga Recall Due to Layer Separation Risk

    Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, posing a risk of exposure to contaminants.

    Product
    T4 Pullover Toga, Regular ; Catalog Number: 0400-750-000 Sterile personal protection garment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1463-2018·2018-05-02

    Integra LifeSciences Recalls Humeral Stem Trials for Breakage Risk

    Integra LifeSciences is recalling 1,619 humeral stem trials for the Titan Modular Shoulder System because they may break during surgery.

    Product
    The humeral stems trials are packaged in a kit for Titan Modular Shoulder System under the following labeling: Catalog Number Product Description TRL092002506 Humeral Stem Trial, 6mm TRL092002507 Humeral Stem Trial, 7mm TRL092002508 Humeral Stem Trial, 8mm TRL092002509…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1503-2018·2018-05-02

    Stryker T4 Pullover Toga Recall Due to Layer Separation

    Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, creating a risk of exposure to contaminants.

    Product
    T4 Pullover Toga, Large; Catalog Number: 0400-760-000 Sterile personal protection garment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1466-2018·2018-05-02

    Zimmer Biomet Recalls Humeral Guide Wire Ball Tips Due to Packaging Seal Failure

    Zimmer Biomet is recalling Humeral Guide Wire Ball Tips because the sterile packaging seal may fail, potentially compromising the device's sterility.

    Product
    Humeral Guide Wire Ball Tip 2.4 mm Diameter 70 cm Length; Item Number: 47-2255-008-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1533-2018·2018-05-02

    BD Vacutainer Blood Collection Set Recalled for Sterility Assurance Failure

    Becton Dickinson is recalling BD Vacutainer Ultra Touch Push Button Blood Collection Sets because they do not meet the labeled sterility assurance level.

    Product
    BD Vacutainer¿ Ultra TouchTM Push Button Blood Collection Set 0.6 x 19 mm x 305 mm 23G x ¿ x 12. Catalog no 367364
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1475-2018·2018-05-02

    Zimmer Biomet Recalls Intramedullary Fixation Guide Wires Due to Packaging Seal Failure

    Zimmer Biomet is recalling ZMS Intramedullary Fixation Smooth Guide Wires because the sterile packaging seal may fail, potentially compromising sterility.

    Product
    ZMS Intramedullary Fixation Smooth Guide Wire 2.4 mm Diameter, 100 cm Length; Item Number: 47-2237-033-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1497-2018·2018-05-02

    Diagnostic Hybrids Recalls MicroVue CIC-C1q EIA Kits Due to Bacterial Contamination

    Diagnostic Hybrids, Inc. is recalling 19 MicroVue CIC-C1q EIA kits because a component was found to contain bacterial contamination.

    Product
    MicroVue CIC-C1q EIA, Model A001. The MicroVue CIC-C1q EIA is for detection of circulating immune complexes (CIC) in human serum or plasma. The MicroVue CIC-C1q EIA is for detection of circulating immune complexes (CIC) in human serum or plasma. In certain disease states…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0716-2018·2018-05-02

    McKesson Recalls Diltiazem HCl Extended-Release Capsules Due to Dissolution Failures

    McKesson Packaging Services is recalling Diltiazem HCl Extended-Release Capsules, 240 mg, because stability testing showed high dissolution results.

    Product
    Diltiazem HCl Extended-Release Capsules, USP 240 mg, 100-count bottles, Rx Only, Mfg. By: Par Pharmaceutical One Ram Ridge Rd Chestnut Ridge, NY 10977. NDC: 63739-016-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0685-2018·2018-05-02

    Time-Cap Recalls Ibuprofen Tablets Due to Odor Complaints

    Time-Cap Laboratories is recalling various strengths of ibuprofen tablets due to odor complaints related to CGMP deficiencies.

    Product
    IBUPROFEN — IBUPROFEN (IBUPROFEN)
    Category
    Drug
    Distribution
    Distributed nationwide