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.

41226–41250 of 82310

  • SevereFDA (Drugs)·D-1172-2018·2018-09-12

    McKesson Recalls Megestrol Acetate Oral Suspension Due to Supra-Potent Drug

    McKesson is recalling 1,531 cartons of Megestrol Acetate Oral Suspension because the drug is supra-potent. The recall is voluntary and nationwide.

    Product
    Megestrol Acetate Oral Suspension, USP 400 mg/mL, 10 mL (10 mL UD cups in boxes of 20 cups), Rx Only, Mfg. By: Par Pharmaceutical One Ram Ridge Rd Chestnut Ridge, NY 10977 Dist. By: McKesson Packaging Services a business unit of McKesson Corporation 7101 Weddington Rd. Concord…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1946-2018·2018-09-12

    Fresh Express Recalls Chopped Romaine Due to Cyclospora Test Result

    Fresh Express is recalling 482 cases of Chopped Romaine 1 lb after a test detected the Cyclospora organism. The product was distributed in 15 U.S. states.

    Product
    Fresh Express Chopped Romaine 1 lb
    Category
    Food
    Distribution
    15 states
  • SevereNHTSA·18V618000·2018-09-12

    Jayco Recalls 2019 Travel Trailers Due to Missing Axle Bearing Races

    Jayco is recalling 2019 White Hawk, Jay Flight, and Jay Flight SLX travel trailers because missing inner bearing races may cause hub overheating and axle separation.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT SLX, JAY FLIGHT, WHITE HAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2959-2018·2018-09-12

    Steris Recalls V-PRO Low Temperature Sterilization Systems Due to Sterilant Expiration Defect

    Steris Corporation is recalling 2,889 V-PRO low temperature sterilization systems because they may fail to detect expired sterilant cups after a power cycle.

    Product
    AMSCO V-PRO 1, V-PRO 1 Plus, and V-PRO maX Low Temperature Sterilization Systems The V-PRO 1, V-PRO 1 Plus, and V-PRO maX Low Temperature Sterilization Systems, using VAPROX HC Sterilant, are intended for use in the terminal Sterilization of properly prepared (cleaned…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2989-2018·2018-09-12

    GE Vivid 7 Ultrasound System Recalled for Power Cord Shock Risk

    GE Medical Systems is recalling 12,426 Vivid 7 ultrasound systems because the power cord may break and expose electrical conductors, creating a shock hazard.

    Product
    GE Vivid 7 ultrasound system Product Usage: Vivid E7 is a general-purpose ultrasound system, specialized for use in cardiac imaging. It is intended for use by, or under the direction of a qualified physician for ultrasound imaging and analysis of Fetal/Obstetrics; Abdominal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2988-2018·2018-09-12

    GE Vivid E95 Ultrasound System Recalled for Power Cord Shock Risk

    GE Medical Systems is recalling 12,426 Vivid E95 ultrasound systems because the power cord may break and expose electrical conductors, creating a shock hazard.

    Product
    GE Vivid E95 ultrasound system Product The device is intended for use by a qualified physician for ultrasound evaluation of Fetal; Abdominal (including renal and GYN); Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2987-2018·2018-09-12

    GE Vivid E90 Ultrasound System Recalled for Electrical Shock Risk

    GE Medical Systems is recalling Vivid E90 ultrasound systems because the power cord may break and expose electrical conductors, posing a risk of shock.

    Product
    GE Vivid E90 ultrasound system Product Usage: Vivid E80 / E90 / E95 ultrasound system is general-purpose ultrasound systems, specialized for use in cardiac imaging. It is intended for use by, or under the direction of a qualified physician for ultrasound imaging and analysis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2984-2018·2018-09-12

    GE LOGIQ 9 Ultrasound System Recalled for Power Cord Shock Risk

    GE Medical Systems is recalling 12,426 LOGIQ 9 ultrasound systems because the power cord may break and expose electrical conductors, creating a shock hazard.

    Product
    GE LOGIQ 9 ultrasound system Product Usage: The device is intended for use by a qualified physician for ultrasound evaluation of Fetal; Abdominal; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2986-2018·2018-09-12

    GE Vivid E80 Ultrasound System Recalled for Power Cord Shock Risk

    GE Medical Systems is recalling Vivid E80, E90, and E95 ultrasound systems because the power cord may break and expose electrical conductors, creating a shock hazard.

    Product
    GE Vivid E80 ultrasound system Vivid E80 / E90 / E95 ultrasound system is general-purpose ultrasound systems, specialized for use in cardiac imaging. It is intended for use by, or under the direction of a qualified physician for ultrasound imaging and analysis of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2983-2018·2018-09-12

    GE LOGIQ E9 Ultrasound System Recalled for Power Cord Shock Risk

    GE Medical Systems is recalling 12,426 LOGIQ E9 ultrasound systems because the power cord side may break, exposing electrical conductors and creating a risk of electric shock.

    Product
    GE LOGIQ E9 ultrasound system Product Usage: The device is intended for use by a qualified physician for ultrasound evaluation of Fetal; Abdominal; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2985-2018·2018-09-12

    GE Vivid E9 Ultrasound System Recalled for Power Cord Shock Risk

    GE Medical Systems is recalling 12,426 Vivid E9 ultrasound systems because the power cord may break and expose electrical conductors, posing a risk of electric shock.

    Product
    GE Vivid E9 ultrasound system Product Usage: GE Vivid E9 ultrasound system is a general purpose ultrasound system for use in cardiac imaging. It is intended for use by, or under direction of a qualified physician for ultrasound imaging and analysis of Fetal; Abdominal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2975-2018·2018-09-12

    Quasar Pure Rayz Light Therapy System Recalled for Uncleared Claims

    Quasar Bio-Tech is recalling 6,783 Pure Rayz Light Therapy Systems because the packaging and manuals make claims about collagen and elastin production that were not cleared by the FDA.

    Product
    Pure Rayz, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2967-2018·2018-09-12

    Encore Medical Recalls Foundation Modular Femoral Stem for Lack of Clearance

    Encore Medical is recalling 12 units of the Foundation Modular Femoral Stem because the device lacks FDA clearance.

    Product
    Foundation Modular Femoral Stem, Part Number, 220-10-110. Knee prosthesis component. The Foundation Revision Knee is a total knee system indicated as knee joint replacement for patients suffering from pain and dysfunction.
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Food)·F-1933-2018·2018-09-12

    Virtus Pharmaceuticals Recalls Virt-Nate and Virt Gard Tablets for Labeling Error

    Virtus Pharmaceuticals is recalling Virt-Nate and Virt Gard tablets because the labels do not reflect the correct amount of Dietary Folate Equivalents.

    Product
    Virt Gard Tablets, Number of units per package: 100 Tablets Package Type: 100 Tablets/Bottle
    Category
    Food
    Distribution
    26 states
  • ModerateFDA (Drugs)·D-1183-2018·2018-09-12

    Akorn Recalls Ethosuximide Capsules Due to Impurity Failures

    Akorn, Inc. is recalling Ethosuximide Capsules, 250 mg, due to out-of-specification results for an unspecified impurity.

    Product
    Ethosuximide Capsules, USP, 250 mg, 100 capsules per bottle, Rx only, Mfg For VersaPharm Incorporated, Maroerre, GA 30062. Mfg By: Swiss Caps AG, Kirchberg, Switzerland. NDC: 61748-025-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2969-2018·2018-09-12

    Inspire II Implantable Pulse Generator Recalled for Incorrect Use-By Date

    Inspire Medical Systems is recalling 93 Inspire II Implantable Pulse Generators because the device registration labels contain an incorrect use-by date.

    Product
    Inspire II Model 3024 Implantable Pulse Generator (IPG) for Obstructive Sleep Apnea, Inspire Part #900-003-020, Product Usage: The device is an implanted component of the Inspire Upper Airway Stimulation (UAS) system. The UAS therapy is used to treat a subset of patients…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2973-2018·2018-09-12

    Quasar Bio-Tech Recalls Baby Quasar Plus Light Therapy System

    Quasar Bio-Tech is recalling the Baby Quasar Plus Light Therapy System because it lacks FDA clearance for specific collagen and elastin claims.

    Product
    Baby Quasar Plus, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1932-2018·2018-09-12

    Virtus Pharmaceuticals Recalls Virt-Nate and Virt Gard Tablets for Labeling Error

    Virtus Pharmaceuticals is recalling Virt-Nate and Virt Gard Tablets because the labels do not reflect the correct amount of Dietary Folate Equivalents.

    Product
    Virt-Nate Tablets, Number of units per package: 100 Tablets Package Type: 100 Tablets/Bottle
    Category
    Drug
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-2974-2018·2018-09-12

    Quasar MD Plus Light Therapy System Recalled for Uncleared Claims

    Quasar Bio-Tech, Inc. is recalling the Quasar MD Plus Light Therapy System because the packaging and user manuals contain claims for collagen and elastin production that were not cleared by the FDA.

    Product
    Quasar MD Plus, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2963-2018·2018-09-12

    Zimmer Dental Implants Recalled for Incorrect Inner Package Labeling

    Zimmer Dental Inc. is recalling 299 units of Tapered Screw-Vent Implants because the inner package labels display incorrect item, lot, and size information.

    Product
    Outer Package Label: Tapered Screw-Vent Implant System, 4.1mm X 10mm, 3.5mm, REF:TSVM4B10, Sterile:R, Rx Only; Inner Package Label: Implant, MTX, 3.7mm x 10mm,3.5mm, REF: TSVB10. Zimmer Dental Implants are designed for use in the maxilla or mandible for immediate loading or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V612000·2018-09-11

    Ford Recalls 2018 Edge and Lincoln MKX for Door Striker Bolt Defect

    Ford is recalling 2018 Ford Edge and Lincoln MKX vehicles because shorter-than-intended door striker bolts may cause doors to open in a crash, increasing injury risk.

    Product
    FORD — FORD, LINCOLN EDGE, MKX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V608000·2018-09-11

    Mercedes-Benz Recalls 2018 C-Class Models Due to Rear Window Bonding Defect

    Mercedes-Benz is recalling 2018 C300, C300 4MATIC, C63 AMG, and C63S AMG vehicles because incorrect rear window bonding may cause the glass to detach, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ AMG C63S, C 300 4MATIC, C 300, AMG C63
    Category
    Vehicle
    Distribution
    Distributed nationwide