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.

Which agencies issued them

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.

51501–51525 of 82328

HighFDA (Devices)·Z-0295-2017·2016-10-26
Ethicon Endo-Surgery Recalls Endoscopic Articulating Linear Cutters Due to Gear Failure
Ethicon Endo-Surgery Inc is recalling 105 Endoscopic Articulating Linear Cutters because a pinion gear could fail, potentially causing a sharps injury to healthcare professionals.
Product
Endoscopic Articulating Linear Cutter, ATB35. Standard 35 MM. The ENDOPATH ETS-Flex Endoscopic Articulating Linear Cutter has application in general, gynecologic, urologic, and thoracic surgery for transection, resection, and/or creation of anastomoses
Category
Medical Device
Distribution
37 states
HighFDA (Drugs)·D-0112-2017·2016-10-26
Supernus Recalls Trokendi XR Capsules Due to Assay Failure
Supernus Pharmaceuticals is recalling Trokendi XR (topiramate) capsules because they failed to meet assay specifications.
Product
TROKENDI XR — TROKENDI XR (TOPIRAMATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0135-2017·2016-10-26
ConMed CORE Trumpet Handpiece Recalled for Potential Sterility Compromise
ConMed is recalling CORE Trumpet Handpieces because packaging creases may create open channels that compromise sterility.
Product
CORE¿ Trumpet Handpiece only, Catalog Number CD8450 The CORE Trumpet (CD81XX, CD83XX, and CD84XX) has applications in gynecological laparoscopy, laparoscopic cholecystectomy and other laparoscopic procedures
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0246-2017·2016-10-26
Windstone Medical Recalls Morris Hysto Pack Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling 186 Morris Hysto Pack kits because the Medtronic disposable gloves included may contain splits or holes that compromise sterility.
Product
Morris Hysto Pack, Kit number PSS3198 and PSS3198(A convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0212-2017·2016-10-26
Windstone Medical Knee Packs Recalled for Potential Sterility Compromise
Windstone Medical is recalling 30 Knee Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.
Product
Knee Pack, Kit number AMS4211 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0136-2017·2016-10-26
Kabobs Mini Deep Dish Mushroom Pizza Recalled for E. coli O121
Kabobs Inc is recalling Mini Deep Dish Mushroom Pizza because it was made with flour contaminated with E. coli O121.
Product
MINI DEEP DISH MUSHROOM PIZZA, 200 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260.
Category
Food
Distribution
27 states
HighFDA (Devices)·Z-0138-2017·2016-10-26
Olympus OER-Pro Endoscope Reprocessor Recall Issued for Cleaning Instructions
Olympus is recalling OER-Pro endoscope reprocessors because instructions may incorrectly suggest skipping precleaning steps. Users must conduct manual cleaning.
Product
OER-Pro Endoscope Reprocessor, Endoscope washer/disinfector
Category
Medical Device
Distribution
50 states
HighCPSC·17021·2016-10-26
H-E-B Recalls Brazos Embossed Star Chairs Due to Fall Hazard
H-E-B is recalling Brazos Embossed Star Chairs because weld defects may cause armrests to detach, posing a fall hazard. No injuries have been reported.
Product
Brazos Embossed Star Chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0125-2017·2016-10-26
X Spine Systems Recalls Calix P PEEK Lumbar System Trial Devices
X Spine Systems is recalling 1,504 Calix P PEEK Lumbar System trial devices because parts may detach and lodge in the surgical site.
Product
Calix P PEEK Lumbar System, PLIF Trial
Category
Medical Device
Distribution
19 states
HighFDA (Devices)·Z-0156-2017·2016-10-26
Windstone Medical Breast Pack Kits Recalled for Sterility Compromise
Windstone Medical Packaging is recalling 505 breast pack kits because the included Medtronic gloves may contain splits or holes that compromise sterility.
Product
Breast Pack, Kit part number AMS3238, AMS3238(A, AMS3691, AMS4419, PSS1541, PSS1784, PSS1784(A, PSS1784(B, PSS2272, and PSS2272(A. convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0142-2017·2016-10-26
Kabobs Recalls Mini Vegetable Springrolls Due to E. coli O121 Contamination
Kabobs Inc is recalling Mini Vegetable Springrolls because they were manufactured with flour contaminated with E. coli O121.
Product
MINI VEGETABLE SPRINGROLL, 200 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260.
Category
Food
Distribution
27 states
HighFDA (Devices)·Z-0160-2017·2016-10-26
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because splits or holes may compromise sterility.
Product
C-Tray Pack, Kit number PSS2707and PSS2707(A convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0200-2017·2016-10-26
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because they may contain splits or holes that compromise sterility.
Product
GYN Lap Pack, Kit number PSS2194(B convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0118-2017·2016-10-26
Merge Healthcare Recalls CADstream Software Due to Incorrect Patient Follow-up
Merge Healthcare is recalling CADstream software versions prior to 5.2.6 because changes to study protocols may result in incorrect patient follow-up.
Product
CADstream software Product Usage: CADstream is an image processing system designed to assist in the visualization, analysis, and reporting of magnetic resonance imaging (MRI) studies. CADstream also is intended to provide workflow efficiency and interventional planning…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0207-2017·2016-10-26
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because splits or holes may compromise sterility in custom surgical kits.
Product
Head Pack, Item number PSS1934(B convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0168-2017·2016-10-26
Windstone Medical Recalls Custom Venous Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling 1,584 Custom Venous Kits because the Medtronic gloves included in the kits may contain splits or holes that compromise sterility.
Product
Custom Venous Kit, TVS4024(C convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0277-2017·2016-10-26
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because they may contain splits or holes that compromise sterility.
Product
Total Knee Pack, Kit number AMS4010(A convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0234-2017·2016-10-26
Windstone Medical Recalls Major Lithotomy Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling Major Lithotomy Packs because the included Medtronic gloves may have splits or holes that compromise sterility.
Product
Major Lithotomy Pack, kit number 002641-5 and 002641-6 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·17706·2016-10-26
Hearth & Home Technologies Recalls Quadra Fire Explorer III Wood Stoves
Hearth & Home Technologies is recalling about 650 Quadra Fire Explorer III wood stoves because the top lid handle can disengage, causing the lid to slam shut on fingers.
Product
Quadra Fire® Explorer III wood stoves
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0230-2017·2016-10-26
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Windstone Medical Packaging is recalling 20 Major Breast Packs containing Medtronic gloves that may have splits or holes, compromising sterility.
Product
Major Breast Pack, Kit number AMS3409 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0237-2017·2016-10-26
Windstone Medical Mammoplasty Kits Recalled for Potential Sterility Compromise
Windstone Medical Packaging is recalling 140 Mammoplasty Kits because the included Medtronic gloves may contain splits or holes that compromise sterility.
Product
Mammoplasty Pack, Kit number AMS2535 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0164-2017·2016-10-26
Windstone Medical Recalls Custom Breast Augmentation Kits Due to Sterility Risk
Windstone Medical Packaging is recalling 546 custom breast augmentation kits because the included Medtronic gloves may contain splits or holes that compromise sterility.
Product
Custom Breast Augmentation Pack, Kit number PSS2455(B, PSS2455(C, PSS2455(D convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0239-2017·2016-10-26
Medtronic Disposable Gloves Recalled for Sterility Compromise in Surgical Kits
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because splits or holes may compromise sterility in custom surgical kits.
Product
Minor Lap Pack, Kit number AMS2624 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0219-2017·2016-10-26
Windstone Medical Recalls Laparoscopic Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 1,290 laparoscopic kits because the disposable gloves included may have splits or holes that compromise sterility.
Product
Laparoscopic Pack, Kit number AMS2499 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0173-2017·2016-10-26
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because splits or holes may compromise sterility in custom surgical kits.
Product
Dr Bragg Vein Tray - RX, kit numbers 007912-5, 007912-6, 007912-7, 007912-8 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide