State

Missouri product recalls

72,820 recalls have nationwide distribution and so reach Missouri. 8,460 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total: 8,460
Critical: 1,333
Severe: 1,869
Most recent: 2026-09-02

Of the 8,460 recalls naming Missouri we have scored against our rubric, 1,333 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,869 (22%) are Severe.

Which agencies issued them

These figures cover only the 8,460 recalls whose distribution notice names Missouri specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

76–100 of 81280

HighFDA (Devices)·Z-3025-2026·2026-09-02
Medline Recalls Gynecologic Robotic Surgery Kits Due to Contamination
Medline Industries is recalling 1,349 gynecologic robotic surgery kits nationwide because they contain a potentially contaminated component.
Product
Medline convenience kits labeled as: 1) GYN ROBOTIC CDS, Medline Kit SKU CDS982888Q; 2) GYN ROBOTIC ADD ON PACK, Medline Kit SKU DYNJ43837D; 3) OH GYN/LAP ROBOT PACK, Medline Kit SKU DYNJ89759; 4) GYN LAPAROSCOPY PACK, Medline Kit SKU DYNJ89781; 5) ROBOT ME RF, Medline
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3031-2026·2026-09-02
Healthmark ProChek-II Medical Tests Recalled for Expired Ingredient
Healthmark Industries is recalling ProChek-II tests because they were manufactured with an expired ingredient, which may cause false negative or positive results.
Product
healthmark ProChek-II, Model Number PT-313, PT-201-12
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2996-2026·2026-09-02
Medline Neurosponge Kits Recalled for Endotoxin Levels
Medline is recalling 3,468 neurosurgical convenience kits containing Pilling Wecksorb Neurosponges due to potential out-of-specification endotoxin levels.
Product
Medline medical convenience kits, labeled as: 1) NEURO CDS, Medline Kit SKU CDS985246J; 2) NEURO PACK, Medline Kit SKU DYNJ32770V; 3) NEURO BUNDLE-LF, Medline Kit SKU DYNJ40095D; 4) NEURO PACK-LF, Medline Kit SKU DYNJ42844D; 5) NEURO PACK, Medline Kit SKU DYNJ45121I;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3028-2026·2026-09-02
Medline Recalls 419 Surgical Kits Due to Contaminated Component
Medline Industries is recalling 419 surgical convenience kits because they contain a potentially contaminated component. The kits were distributed nationwide.
Product
Medline convenience kits labeled as: 1) CMH LITHO MINOR PACK-LF, Medline Kit SKU DYNJ54362F; 2) EAST MAJOR LITHOTOMY, Medline Kit SKU DYNJ900957C; 3) GYN LAPAROTOMY, Medline Kit SKU DYNJ906804B; 4) UNIVERSAL GYN, Medline Kit SKU DYNJ910195A.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0777-2026·2026-09-02
Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 75 mcg tablets nationwide because they may contain less than the labeled amount of active ingredient.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3014-2026·2026-09-02
Canon Medical Alphenix X-ray Systems Recalled for Loose Ceiling Screws
Canon Medical System, USA, INC. is recalling 10 Alphenix digital radiography systems because fixing screws in the ceiling suspended arm may become loose.
Product
Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for blood vessels in the he
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3032-2026·2026-09-02
Healthmark Protein Test Recalled Due to Expired Ingredient
Healthmark is recalling ProChek protein tests because they were manufactured with an expired ingredient, which may cause false negative or positive results.
Product
healthmark ProChek-W Protein Test for Robotic Arms; ProChek-Semi Quantitative Protein Test, Model Number PT-SQ-001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3023-2026·2026-09-02
Medline Convenience Kits Recalled for Potentially Contaminated Component
Medline Industries is recalling 15 convenience kits (SKU CDS980375M) due to a potentially contaminated component. The kits were distributed in 18 US states.
Product
Medline convenience kits labeled as: LTP CDS-LF, Medline kit SKU CDS980375M
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0782-2026·2026-09-02
Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide
Accord Healthcare is recalling specific lots of Levothyroxine Sodium 137 mcg tablets because they may contain less than the labeled amount of active ingredient.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3017-2026·2026-09-02
Fresenius BlueStar Hemodialysis Machines Recalled for Alarm Defects
Fresenius Medical Care is recalling 1,140 BlueStar Hemodialysis machines due to reported flow, water, or temperature-related alarms.
Product
Fresenius Medical Care, 2008T BlueStar Hemodialysis Machine, Model Numbers: 191126, 191130.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3034-2026·2026-09-02
IMRIS ORT300 Operating Room Table Recalled for Mechanical Failure Risk
IMRIS Imaging Inc is recalling 13 ORT300 operating room tables because a mechanical failure could cause unintended rotational movement, posing a risk of injury to patients.
Product
ORT300, operating room table, ORT300 Modular Table Main Unit Assy Part Numbers 114093-000 and 114093-600
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0781-2026·2026-09-02
Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 125 mcg tablets because they are subpotent. The recall is ongoing nationwide.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·26V570000·2026-09-02
Toyota Recalls 2026 C-HR Vehicles Due to Battery Overcharge Risk
Toyota is recalling 8,521 2026 C-HR battery electric vehicles because a software error may cause the battery to overcharge, potentially leading to a loss of drive power and increased crash risk.
Product
TOYOTA — TOYOTA C-HR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2995-2026·2026-09-02
Medline Medical Convenience Kits Recalled for Endotoxin Levels
Medline is recalling 246 surgical convenience kits containing neurosponges due to potential out-of-specification endotoxin levels.
Product
Medline medical convenience kits, labeled as: 1) CRANIOTOMY PACK, Medline Kit SKU DYNJT6545; 2) ORTHO SPINE PACK, Medline Kit SKU DYNJ88056A; 3) ENT SINUS PACK, Medline Kit SKU DYNJ89001; 4) THYROID ENT, Medline Kit SKU DYNJ908641.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0784-2026·2026-09-02
Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium tablets because they may contain less active ingredient than labeled.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-1278-2026·2026-09-02
Byron White Herbal Supplement Recalled for Undeclared Walnut Allergen
Byron White Formulas is recalling its A-FNG Herbal Supplement because the label fails to declare walnuts in English, posing a risk to consumers with nut allergies.
Product
Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404
Category
Food
Distribution
50 states
ModerateFDA (Devices)·Z-3011-2026·2026-09-02
Halyard Total Joint Kits Recalled for Latex Labeling Deficiency
AVID Medical is recalling 78 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
Product
Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3002-2026·2026-09-02
American Contract System Convenience Kits Recalled for Performance Failures
American Contract Systems Inc is recalling 30 units of Convenience Kits because Medline catheters failed performance specifications.
Product
American Contract System Convenience Kits, CV B PACK, Model/Catalog Number: TNCB10AP
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3003-2026·2026-09-02
American Contract System Convenience Kit Recalled for Performance Failures
American Contract Systems Inc is recalling 12 Convenience Kits containing Medline catheters because samples failed performance specifications.
Product
American Contract System Convenience Kit, D & C PACK, Model/Catalog Number: LLPD90H
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3035-2026·2026-09-02
Olympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
Olympus is recalling 335 PowerSeal 5 mm Sealer & Divider devices because the outer shelf box is incorrectly labeled as a 37-cm device.
Product
POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action. GEI / Electrosurgical, cutting & coagulation & accessories
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3006-2026·2026-09-02
AVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
AVID Medical is recalling 63 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.
Product
Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0831-2026·2026-09-02
Hikma Recalls Ramipril Capsules Due to Process Impurity
Hikma Pharmaceuticals is recalling specific lots of Ramipril 10 mg capsules because they failed impurity specifications for dicyclohexylurea.
Product
RAMIPRIL — RAMIPRIL (RAMIPRIL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0783-2026·2026-09-02
Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 150 mcg tablets because they may contain less active ingredient than labeled.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3018-2026·2026-09-02
ConMed Suture Anchor Recalled for Incorrect Patient Implant Card
ConMed is recalling specific suture anchors because they may contain incorrect patient implant cards, which could lead to incorrect device identification and traceability.
Product
CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Suture Anchor with two, #2 (5 metric) Hi-Fi Sutures Sterile
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3030-2026·2026-09-02
Fujifilm Synapse PACS Software Recalled for Inaccurate Ruler Measurements
Fujifilm is recalling Synapse PACS software v7.4.310 because a software issue may cause ruler measurements to be inaccurate.
Product
FUJIFILM Synapse PACS software v7.4.310; radiological image processing system
Category
Medical Device
Distribution
Distributed nationwide