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.

676–700 of 81280

HighFDA (Devices)·Z-2728-2026·2026-07-22
Mobile Digital Radiographic System Arm Drop Risk During Patient Exams
GE HealthCare is recalling certain Optima XR200/220/240amx Mobile Digital Radiographic Systems due to potential failure of the Column Safety mechanism, which could cause the X-ray arm to drop during patient exams. The issue stems from incomplete functional testing of the safety pawl after column replacement.
Product
Optima XR240amx, Mobile Digital Radiographic System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2721-2026·2026-07-22
Olympus Glass Body for 194 Ellik Evacuator Model 190A Sterilization Recall
Olympus Corporation is recalling the Glass Body for 194 Ellik Evacuator (Model 190A) because certain sterilization parameters in the instructions may not consistently render the devices adequately sterile.
Product
Olympus Glass Body for 194 Ellik Evacuator. Model Number: 190A.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2725-2026·2026-07-22
Rapid Refill Continuous Injection System Recalled for Syringe Loosening Risk
Boston Scientific's Rapid Refill Continuous Injection System (UPN M00566001) is being recalled because the recalled Medline Namic Angiographic Control Syringe may loosen or disconnect from the manifold, potentially causing leakage, inability to aspirate or inject, and procedure delays.
Product
Rapid Refill Continuous Injection System, UPN M00566001
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0684-2026·2026-07-22
Good Neighbor Pharmacy Earwax Removal Drug Recalled for Low Potency
Bell Pharmaceuticals is recalling Good Neighbor Pharmacy Earwax Removal (Carbamide Peroxide 6.5%) due to subpotency—the active ingredient concentration is significantly reduced from expected levels, and the product has a low pH.
Product
GOOD NEIGHBOR PHARMACY EARWAX REMOVAL — GOOD NEIGHBOR PHARMACY EARWAX REMOVAL (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2746-2026·2026-07-22
Tosoh ST AIA-Pack Testosterone Diagnostic Test Kit Recall
Tosoh Bioscience is recalling ST AIA-Pack Testosterone test kits due to low-quality control results that could produce falsely elevated or falsely low testosterone measurements, potentially leading to unnecessary testing or delayed diagnosis.
Product
ST AIA-Pack Testosterone, IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of testosterone in human serum on specific Tosoh AIA System analyzers, Model Number 0025204
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0685-2026·2026-07-22
Leader Carbamide Peroxide Earwax Removal Kit Recalled for Subpotency
Bell Pharmaceuticals is recalling Leader Carbamide Peroxide 6.5% Earwax Removal Kit due to subpotency—the active ingredient is significantly reduced (approximately 0.6% versus the expected 6–7%) and the pH is low.
Product
LEADER EARWAX REMOVAL KIT EARWAX REMOVAL AID AND BULB — LEADER EARWAX REMOVAL KIT EARWAX REMOVAL AID AND BULB (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2742-2026·2026-07-22
Photera 400 Phototherapy Device Recalled for Incorrect UV Sensor Calibration
Daavlin Distributing Company is recalling the Photera 400 phototherapy device because the UV sensor calibration is calculating incorrectly, resulting in lower output levels than intended.
Product
Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2722-2026·2026-07-22
da Vinci SP Instrument Arm Drape may detach during surgical procedures
Intuitive Surgical is recalling da Vinci SP Instrument Arm Drapes because the drape rings may detach, exposing the instrument arm and potentially delaying procedures. The recall affects 11,113 units distributed worldwide.
Product
da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0680-2026·2026-07-22
Quality Choice Earwax Removal Kit Carbamide Peroxide Subpotent Drug Recall
Bell Pharmaceuticals is recalling Quality Choice Earwax Removal Kit (Carbamide Peroxide 6.5%) due to subpotent drug content, with assay levels significantly reduced (approximately 0.6% versus expected 6–7%) and low pH levels.
Product
QUALITY CHOICE EARWAX REMOVAL KIT — QUALITY CHOICE EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0686-2026·2026-07-22
Foster & Thrive Carbamide Peroxide 6.5% Recalled for Subpotent Strength
Bell Pharmaceuticals recalls Foster & Thrive Carbamide Peroxide 6.5% due to subpotent drug substance with low pH and significantly reduced assay levels. Approximately 31,094 units distributed nationwide are affected.
Product
Foster & Thrive, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), NDC 70677-1154-01, Distributed by: McKesson Corp., via SSSL, Memphis, TN 38141.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2734-2026·2026-07-22
Papablic Replacement Brush Heads Recalled Due to Breakage Risk
Papablic Inc is recalling Papablic Replacement Brush Heads (Model PAPA317AA) due to potential for brush heads to break. The recall affects approximately 13,400 packs distributed nationwide.
Product
Papablic Replacement Brush Heads. Model Number: PAPA317AA.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2743-2026·2026-07-22
Photera 600 Phototherapy Device UV Sensor Calibration Error
Daavlin Distributing Company is recalling 26 Photera 600 phototherapy devices nationwide because the UV sensor gain calibration is incorrect, causing inaccurate ultraviolet output readings.
Product
Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2731-2026·2026-07-22
Orthofix Articulated Minirail Fixator devices recalled for incorrect labeling
Orthofix U.S. LLC is recalling Articulated Minirail Fixator external fixation devices due to incorrect model labeling. Three models were mislabeled: M101 labeled as M103, M103 labeled as M101, and M122 labeled as M111.
Product
Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS REF: M111, Unilateral orthopedic/trauma external fixation device
Category
Medical Device
Distribution
26 states
ModerateFDA (Food)·H-1152-2026·2026-07-22
Liquid Hope Organic Meal Replacement Formula Subpotent Vitamin A Recall
Nutricia North America is recalling Liquid Hope Organic Whole Foods Meal Replacement Peptide Formula Berry Medley because the product contains less vitamin A than labeled. A testing laboratory used an incorrect method that overstated the vitamin A concentration.
Product
functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ (341g) case UPC 8 57858 00453 3, package UPC 8 57858 00450 2
Category
Food
Distribution
49 states
ModerateFDA (Drugs)·D-0687-2026·2026-07-22
Meijer Earwax Removal Kit Recalled for Subpotent Active Ingredient
Bell Pharmaceuticals is recalling Meijer Earwax Removal Kit (Carbamide Peroxide 6.5%) due to subpotency: the product contains significantly reduced active ingredient (~0.6% vs. expected ~6–7%) and low pH, limiting effectiveness.
Product
MEIJER EARWAX REMOVAL KIT — MEIJER EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0688-2026·2026-07-22
CAREone Earwax Removal Drops Recalled for Subpotent Active Ingredient
CAREone Earwax Removal Drops (Carbamide Peroxide 6.5%) are recalled because the product contains significantly reduced active ingredient (~0.6% vs. expected ~6–7%) and low pH, making it ineffective.
Product
CAREONE EARWAX REMOVAL DROPS — CAREONE EARWAX REMOVAL DROPS (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0677-2026·2026-07-22
Nystatin Cream Recall Due to Low Potency Test Results
Padagis US LLC is recalling Nystatin Cream USP (100,000 USP units) because long-term stability testing found assay results below specification, meaning the product may contain less active ingredient than labeled.
Product
NYSTATIN — NYSTATIN (NYSTATIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2732-2026·2026-07-22
Orthofix MINIRAIL External Fixation Devices Incorrectly Labeled
Orthofix MINIRAIL unilateral external fixation devices may be labeled with incorrect model numbers. Three model variants (M101, M103, M122) were mislabeled during manufacturing.
Product
Orthofix MINIRAIL, ARTICULATED, FIXATOR, VERTICAL AXIS REF: M122, Unilateral orthopedic/trauma external fixation device
Category
Medical Device
Distribution
26 states
ModerateFDA (Devices)·Z-2733-2026·2026-07-22
Papablic Replacement Brush Heads Recalled for Potential Breakage
Papablic Inc is recalling certain Papablic18B replacement brush head packs because the brush heads may break during use.
Product
Papablic Replacement Brush Heads. Model Number: Papablic18B
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2744-2026·2026-07-22
Photera 600 3-D phototherapy device UV sensor calibration error recall
Daavlin Distributing Company is recalling Photera 600 3-D phototherapy devices because the UV sensor gain calculation is incorrect, causing inaccurate ultraviolet output measurement.
Product
Photera 600 3-D, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0683-2026·2026-07-22
Family Wellness Carbamide Peroxide Earwax Removal Kit Subpotent Drug
Family Wellness Carbamide Peroxide 6.5% earwax removal kits are being recalled because they are subpotent with low pH and significantly reduced active ingredient content (approximately 0.6% versus the expected 6–7%). Consumers should stop using affected lots and consult their pharmacist.
Product
FAMILY WELLNESS EARWAX REMOVAL EARWAX AND BULB — FAMILY WELLNESS EARWAX REMOVAL EARWAX AND BULB (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0682-2026·2026-07-22
Audiologist's Choice Carbamide Peroxide Earwax Removal Recalls
Bell Pharmaceuticals is recalling Audiologist's Choice Carbamide Peroxide earwax removal product due to subpotency: the active ingredient concentration is approximately 0.6% instead of the expected 6–7%, and the product has low pH.
Product
AUDIOLOGISTS CHOICE EARWAX REMOVAL SYSTEM — AUDIOLOGISTS CHOICE EARWAX REMOVAL SYSTEM (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1153-2026·2026-07-22
Nutricia NOURISH Organic Meal Replacement Powder Recalled for Low Vitamin A
Nutricia North America is recalling its NOURISH ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY because testing showed the product contains less vitamin A than the label states. A laboratory error led to inaccurate test results that overstated the actual vitamin A concentration in the product.
Product
functional formularies NOURISH ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY COMPLETE PLANT BASED NUTRITION NET WT. 12 OZ (341g) case UPC 8 57858 00445 8, package UPC 8 57858 00447 2
Category
Food
Distribution
49 states
ModerateFDA (Devices)·Z-2729-2026·2026-07-22
Orthofix MINIRAIL external fixation devices recalled for incorrect model labeling
Orthofix U.S. LLC is recalling Orthofix MINIRAIL external fixation devices (Model M101) because they may be labeled with incorrect model numbers, potentially leading to use of wrong device specifications.
Product
Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number: M101, Unilateral orthopedic/trauma external fixation device
Category
Medical Device
Distribution
26 states
ModerateFDA (Food)·H-1174-2026·2026-07-22
Amy's Organic Lentil Soup Recalled for Potential Spoilage Risk
Amy's Kitchen is recalling Amy's Organic Soups Lentil Light in Sodium (14.5 oz cans) due to potential for spoilage. The recall affects approximately 15,350 cases distributed across multiple U.S. states and Canada.
Product
Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ. (411 g) Microwave: Place soup in a microwave-safe bowl. Cover. Cook for 1.5-2 minutes. Let sit 1 minute. Stir. Serve. Stovetop: Heat soup in a saucepan, stirring occasionally. AMY'S KITCHEN, INC. P.O. BOX 7129 PETAL
Category
Food
Distribution
28 states