State

Missouri product recalls

73,576 recalls have nationwide distribution and so reach Missouri. 8,496 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total: 8,496
Critical: 1,344
Severe: 2,198
Most recent: 2026-10-14

Of the 8,496 recalls naming Missouri we have scored against our rubric, 1,344 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,198 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,496 recalls whose distribution notice names Missouri specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26051–26075 of 82072

ModerateFDA (Devices)·Z-2393-2021·2021-09-08
Steripath Luer Transport Pack Gen2 Recalled for Incorrect Instructions
Magnolia Medical Technologies is recalling 9,400 units of Steripath Luer Transport Pack Gen2 because they were shipped with incorrect Transfer Adapter Instructions For Use (IFU).
Product
Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This holder/adapter assembly may be used for the access of a specimen from Catheter Port to BD Vacutainer¿ Blood Collection or Urine Collection Tubes.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2407-2021·2021-09-08
COVID-19 diagnostic test distributed outside certified laboratory channels
CareStart COVID-19 Antigen Rapid Diagnostic Test units were distributed to non-CLIA-certified customers, violating the product's Emergency Use Authorization requirements.
Product
CareStart COVID-19 Antigen Rapid Diagnostic Test for the detection of SARS-CoV-2 Antigen Qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal or anterior nasal swab specimens directly collected from individuals suspected of COVID-19 by…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0785-2021·2021-09-08
Lidocaine Ointment USP 5% Recalled for Failed Viscosity Specifications
Teligent Pharma is recalling Lidocaine Ointment USP 5% (114,456 tubes, Lots 15378 and 14418) distributed nationwide because certain lots do not meet viscosity specifications, as determined through routine testing.
Product
Lidocaine Ointment USP, 5% Rx Only, Net Wt 35.44 g(1 1/4 oz)packaged in a laminat tube, Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-008-14.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0784-2021·2021-09-08
Donepezil HCL Tablets 5 mg Recalled for Subpotency
Jubilant Cadista Pharmaceuticals is recalling Donepezil HCL Tablets, USP, 5 mg (Lot # DN120006A, exp. 12/2021) because the tablets are subpotent—meaning they contain less active ingredient than specified. The recall affects 14,544 bottles distributed nationwide.
Product
Donepezil HCL Tablets, USP, 5 mg, 90-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd. India, Marketed by: Jubilant Cadista Pharmaceuticals Inc. Salisbury, MD 21801 NDC 59746-329-90
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V694000·2021-09-07
Eldorado EZRM Recalled for Fuel Hose Leak Fire Risk
Eldorado National is recalling 2019-2021 EZRM vehicles with L9 Diesel Engines due to a fuel hose leak that increases fire risk.
Product
ELDORADO — ELDORADO EZRM
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V693000·2021-09-07
LDJ Recalls 2021 Thunder Creek Trailers Due to Fender Light Wiring Defect
LDJ Manufacturing is recalling 279 2021 Thunder Creek trailers because improperly routed wiring may cause fender clearance lights to fail, increasing crash risk.
Product
THUNDER CREEK — THUNDER CREEK STT, MTO, SLT, MTT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21E084000·2021-09-04
Nineo F2-H11 LED Bulbs Recalled for Excessive Brightness
Nineo is recalling F2-H11 replacement LED bulbs because they may be too bright, posing a glare hazard to oncoming drivers.
Product
EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V691000·2021-09-03
2021 Forest River Berkshire RVs Recalled for Electrical Fire Risk
Forest River is recalling certain 2021 Berkshire recreational vehicles that may have unsealed mini-breakers in the electrical system, which could cause sparks and increase the risk of fire in the battery compartment.
Product
FOREST RIVER — FOREST RIVER BERKSHIRE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21E083000·2021-09-03
Cummins Recalls Electric Drivetrain Systems Due to Shutdown Override Failure
Cummins is recalling specific electric drivetrain systems where the high-voltage shutdown override switch may fail to function, increasing crash risk.
Product
ELECTRICAL SYSTEM recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V692000·2021-09-03
2021-2022 Coachmen Nova motorhomes recalled for improper battery installation
Forest River is recalling 2021-2022 Coachmen Nova motorhomes because the Absorbed Glass Mat battery was incorrectly installed, allowing hydrogen gas to accumulate inside the vehicle and create a risk of injury.
Product
COACHMEN — COACHMEN NOVA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V686000·2021-09-02
Highland Ridge RV Recalls 1,157 Units Due to Propane Regulator Failure
Highland Ridge RV is recalling 1,157 recreational vehicles because a propane regulator may fail, causing increased pressure and fire risk.
Product
HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW OPEN RANGE, OPEN RANGE ULTRA LITE, OPEN RANGE LIGHT, SILVERSTAR LIMITED
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V688000·2021-09-02
Toyota Tundra vehicles recalled due to headlight electrical circuit fire risk
Certain 2018-2021 Toyota Tundra vehicles have a headlight electrical circuit defect that may power high and low beams simultaneously, causing connector overheating and fire risk. Owners should contact Toyota or NHTSA for remedy information.
Product
TOYOTA — TOYOTA TUNDRA
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21778·2021-09-02
Step2 StepUp Sidekick Learning Towers Recalled Due to Fall Hazard
The Step2 Company is recalling StepUp Sidekick Learning Towers because the storage tray with cup holders and step can come loose, posing a fall hazard to children. Step2 has received 20 reports of the component coming loose, including one report of minor bruises from a fall.
Product
StepUp Sidekick Learning Towers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21V689000·2021-09-02
Freightliner Cascadia trucks recalled for potential steering linkage separation
Daimler Trucks North America is recalling 2019-2021 Freightliner Cascadia trucks due to improperly tightened drag link taper joints that could separate from the steering arm. Loss of steering control could result, increasing crash risk.
Product
FREIGHTLINER — FREIGHTLINER CASCADIA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V681000·2021-09-02
Indian Recalls 2020 Scout Bobber Sixty for Inoperable Brake Lights
Indian Motorcycle is recalling 2020 Scout Bobber Sixty models because an ECU update may have disabled brake lights, increasing crash risk.
Product
INDIAN — INDIAN SCOUT BOBBER SIXTY
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V687000·2021-09-02
2021 Starcraft Telluride RV Propane Regulator Failure Fire Risk
Starcraft is recalling certain 2021-2022 recreational vehicles with defective Winntec propane regulators that may fail, causing increased pressure and larger flames in gas appliances, raising fire risk.
Product
STARCRAFT RV FW — STARCRAFT RV FW, STARCRAFT RV TT TELLURIDE, SUPER LITE, AUTUMN RIDGE OUTFITTER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V690000·2021-09-02
Honda Recalls 2019-2020 CB500X and CBR500R Motorcycles for Brake Defect
Honda is recalling 2019-2020 CB500X and CBR500R motorcycles because excessive grease in the ABS modulator may cause a brake fluid leak, increasing crash risk.
Product
HONDA — HONDA CB500X, CBR500R
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V685000·2021-09-02
Jayco Recreational Vehicles Recalled for Propane Regulator Fire Risk
Jayco is recalling certain 2017-2022 recreational vehicles with Winntec propane regulators that may fail and increase propane pressure, raising the risk of fire in gas appliances.
Product
JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, JAYCO TRAVEL TRAILER, JAYCO SEISMIC, JAY FEATHER, EAGLE, redundant SEISMIC
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2285-2021·2021-09-01
Monoject Sodium Chloride Flush Syringes Recalled for Air Embolism Risk
Cardinal Health recalls 267 million Monoject 0.9% Sodium Chloride Flush Syringes due to a plunger defect that may reintroduce air into the syringe, posing a risk of air embolism during IV administration.
Product
Monoject 0.9% Sodium Chloride Flush Syringe, 3 mL Fill, STERILE, Product Code 8881570123 The proposed device is indicated for use in flushing compatible intravenous tubing systems and indwelling intravascular access devices.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0765-2021·2021-09-01
Fludarabine Phosphate Injection Recalled Due to Sterility Concern
Custopharm, Inc. is recalling Fludarabine Phosphate for Injection, USP 50 mg because the manufacturer detected microbial contamination during environmental monitoring in aseptic manufacturing areas, raising sterility assurance concerns.
Product
FLUDARABINE PHOSPHATE FOR INJECTION, USP, 50 mg per vial, Single dose vial, Rx Only, Mfd for: Leucadia Pharmaceuticals Carlsbad, CA 92011 U.S.A, NDC 24201-237-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2286-2021·2021-09-01
Sodium Chloride Flush Syringe Recalled Due to Plunger Malfunction Risk
Cardinal Health is recalling Monoject 0.9% Sodium Chloride Flush Syringes because the plunger may draw back after use and reintroduce air into the syringe.
Product
Monoject 0.9% Sodium Chloride Flush Syringe, 5mL Fill, STERILE, Product Code 8881570125 The proposed device is indicated for use in flushing compatible intravenous tubing systems and indwelling intravascular access devices.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0768-2021·2021-09-01
SterRx Sodium Bicarbonate in 5% Dextrose Injection Recalled for Sterility Concerns
SterRx is recalling Sodium Bicarbonate in 5% Dextrose Injection (1,000 mL bags) nationwide due to lack of assurance of sterility. Patients using affected lots should consult their healthcare provider immediately.
Product
Sodium Bicarbonate in 5% Dextrose Injection, 150 mEq per 1,000 mL (12.6 mg per mL), 1,000 mL bags, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0767-2021·2021-09-01
SterRx Sodium Bicarbonate Injection Recalled for Non-Sterility
SterRx is recalling Sodium Bicarbonate in 5% Dextrose Injection due to microbial contamination confirmed by third-party laboratory testing. The affected product is a prescription intravenous injection distributed nationwide.
Product
Sodium Bicarbonate in 5% Dextrose Injection, 150 mEq per 1,000 mL (12.6 mg per mL), 1,000 mL bags, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903 NDC 70324-326-01
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V684000·2021-09-01
Mack Recalls 2020-2022 MD Trucks Due to Brake Pedal Defect
Mack is recalling 2020-2022 MD trucks because a defective cotter pin may leave the brake pedal unsecured, increasing crash risk.
Product
MACK — MACK MD
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2284-2021·2021-09-01
Monoject flush syringe recall: plunger may reintroduce air into IV lines
Cardinal Health Monoject flush syringes may have a defect allowing the plunger to draw back and reintroduce air into the syringe. The FDA issued a Class I recall for over 267 million units distributed nationwide.
Product
Monoject 0.9% Sodium Chloride Flush Syringe, 10 mL Fill, STERILE, Product Code 8881570121 The proposed device is indicated for use in flushing compatible intravenous tubing systems and indwelling intravascular access devices.
Category
Medical Device
Distribution
Distributed nationwide