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.

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.

36726–36750 of 82241

  • SevereFDA (Devices)·Z-1210-2019·2019-07-03

    Becton Dickinson Recalls SmartSite Syringe Administration Sets Due to Leaking

    Becton Dickinson is recalling SmartSite Syringe Administration Sets because they may leak, potentially interrupting infusions or exposing healthcare workers to fluids.

    Product
    SmartSite Syringe Administration Set-Product Package Size 50, Catalog Number: 10798696
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1433-2019·2019-07-03

    Pramipexole Dihydrochloride Tablets Recalled for GMP Deviations and Cross-Contamination Risk

    American Health Packaging is recalling Pramipexole Dihydrochloride Tablets due to GMP deviations and a cleaning procedure failure that may have caused cross-contamination.

    Product
    Pramipexole Dihydrochloride Tablets, 0.5 mg, 30 Tablets (6 tablets per blister card), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217 NDC Blister Card: 68084-974-95; NDC Carton: 68084-974-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1430-2019·2019-07-03

    Diphenhydramine Liquid Recalled for Potential Microbial Contamination

    H J Harkins Company is recalling Diphenhydramine HCL Liquid due to potential contamination with Burkholderia cepacia and Ralstonia pickettii.

    Product
    Diphenhydramine HCL Liquid, 12.5 mg/5 mL, 4 oz bottle, Manufactured by Torrent Pharma, Inc., Levittown, PA 19057, NDC 52959-0123-03.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1422-2019·2019-07-03

    Premier Pharmacy Labs Recalls Neostigmine Methylsulfate Syringes for Sterility Concerns

    Premier Pharmacy Labs is recalling Neostigmine Methylsulfate syringes nationwide due to FDA findings of insufficient environmental controls and lack of sterility assurance.

    Product
    Neostigmine Methylsulfate, 5mg/5mL (1mg/mL), 5mL Single Dose Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-234-15, barcode 5 69623 23415 0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1423-2019·2019-07-03

    Premier Pharmacy Labs Recalls Orphenadrine Citrate Syringes Due to Sterility Concerns

    Premier Pharmacy Labs is recalling 4,363 syringes of Orphenadrine Citrate Sterile Injectable Solution because FDA inspections found insufficient environmental controls that may compromise sterility.

    Product
    Orphenadrine Citrate Sterile Injectable Solution *Contains Sulfites*, 30mg/mL, 1mL Sterile Single-Use Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-104-10, barcode 7 69623 10410 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1888-2019·2019-07-03

    Ethicon ENSEAL X1 Curved Jaw Tissue Sealer Recalled for Bleeding Risk

    Ethicon Endo-Surgery Inc is recalling ENSEAL X1 Curved Jaw Tissue Sealers due to reported intraoperative bleeding.

    Product
    Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 25cm Shaft PRODUCT CODE: NSLX125C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V513000·2019-07-03

    BMW Recalls Multiple Models for High Pressure Fuel Pump Defect

    BMW is recalling specific 2019-2020 models because a high pressure fuel pump may not be properly attached, potentially causing a fuel leak and fire risk.

    Product
    BMW — BMW X5, M5, M850I, X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1413-2019·2019-07-03

    Premier Pharmacy Labs Recalls Chlorpromazine Injection Due to Sterility Concerns

    Premier Pharmacy Labs is recalling 824 vials of Chlorpromazine HCL Injection because an FDA inspection found insufficient environmental controls that may compromise sterility.

    Product
    ChlorproMAZINE HCL INJ, 25mg/mL, *Contains Sulfites*, 1mL in a 5mL Sterile SDV, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-122-28, barcode 7 69623 12228 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1415-2019·2019-07-03

    Premier Pharmacy Labs Recalls Droperidol Syringes Due to Sterility Concerns

    Premier Pharmacy Labs is recalling 2,315 syringes of Droperidol Injectable Sterile Solution because FDA inspections found insufficient environmental controls and lack of sterility assurance.

    Product
    Droperidol Injectable Sterile Solution, 0.625mg/mL, 1mL in a 3mL Sterile Single-Use Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-185-10, barcode 0 69623 18510 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1500-2019·2019-07-03

    Hank's Cheesecakes Recalled for Missing Allergen and Ingredient Labels

    Hank's Cheesecakes, LLC is recalling 207 LoRusso Cakes because they were distributed without labels indicating ingredients or major food allergens.

    Product
    LoRusso Cake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1494-2019·2019-07-03

    Hank's Key Lime Cheesecakes Recalled for Missing Allergen Labels

    Hank's Cheesecakes is recalling 207 Key Lime Cheesecakes because they were distributed without labels indicating ingredients or major food allergens.

    Product
    Key Lime Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1514-2019·2019-07-03

    Hank's Neapolitan Cheesecakes Recalled for Missing Allergen Labels

    Hank's Cheesecakes is recalling Neapolitan cheesecakes because the packaging lacks ingredient and major food allergen labels.

    Product
    Neapolitan Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1879-2019·2019-07-03

    GE Healthcare Recalls Replacement ECG Leadwires Due to Defibrillation Risk

    GE Healthcare is recalling 58,045 replacement ECG leadwires worldwide because they may reduce energy delivery during defibrillation, potentially limiting the success of the procedure.

    Product
    Replacement ECG leadwires with snap ends REF/Catalog Number Description 2106386-101 Replacement ECG Leadwire, snap, LL, AHA, 130 cm/ 51 in The reusable ECG leadwire sets enable ECG monitoring with GE equipment requiring rectangular 11-pin ECG trunk cable. Use leadwire sets…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1508-2019·2019-07-03

    Hank's Dreamsicle Cheesecake Recalled for Missing Allergen Labels

    Hank's Cheesecakes is recalling Dreamsicle Cheesecakes because the packaging lacks ingredient and major food allergen information.

    Product
    Dreamsicle Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1852-2019·2019-07-03

    Maquet VOLISTA Surgical Lights Recalled for Coating Crack Risk

    Maquet is recalling two VOLISTA StandOP Surgical Lights because the light head coating may crack, posing a risk of particles falling into the surgical field.

    Product
    Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811901 Model: VLT600SF AIM STP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1859-2019·2019-07-03

    Maquet VOLISTA Surgical Lights Recalled for Coating Crack Risk

    Maquet is recalling 12 VOLISTA StandOP Surgical Lights because light head fork coatings may crack, posing a risk of particles falling into the surgical field.

    Product
    Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229002A Model: VST66SF AIM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1855-2019·2019-07-03

    Maquet VOLISTA Surgical Lights Recalled Due to Coating Crack Risk

    Maquet is recalling 46 VOLISTA StandOP Surgical Lights because light head fork coatings may crack, risking particle contamination in the surgical field.

    Product
    Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811961 Model: VLT600DF AIM STP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1498-2019·2019-07-03

    Hank's Cheesecakes Recalls Turtle Cheesecakes Lacking Allergen Labels

    Hank's Cheesecakes, LLC is recalling 207 Turtle Cheesecakes because they were distributed without labels indicating ingredients or major food allergens.

    Product
    Turtle Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1512-2019·2019-07-03

    Hank's Tiramisu Cheesecake Recalled for Missing Allergen Labels

    Hank's Cheesecakes is recalling Tiramisu Cheesecakes because the packaging lacks ingredient and major food allergen information.

    Product
    Tiramisu Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1510-2019·2019-07-03

    Hank's Cheesecakes Recalls Chocolate Raspberry Cakes for Missing Allergen Labels

    Hank's Cheesecakes, LLC is recalling 207 chocolate raspberry cakes because they were distributed without labels indicating ingredients or major food allergens.

    Product
    Chocolate Raspberry Cake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1507-2019·2019-07-03

    Hank's Blueberry Cheesecakes Recalled for Missing Allergen Labels

    Hank's Cheesecakes is recalling 207 blueberry cheesecakes because they lack labels indicating ingredients and major food allergens.

    Product
    Blueberry Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1493-2019·2019-07-03

    Hank's Cheesecakes Recalled for Missing Allergen and Ingredient Labels

    Hank's Cheesecakes, LLC is recalling plain cheesecakes distributed in Missouri and Illinois because the packages lack labels indicating ingredients or major food allergens.

    Product
    Plain Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states