State

Missouri product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45026–45050 of 82318

ModerateFDA (Drugs)·D-0140-2018·2018-01-03
SSM St. Clare Recalls Morphine PCA Cartridges Due to Sterility Concerns
SSM St. Clare Health Center is recalling specific lots of compounded Morphine PCA cartridges due to a lack of sterility assurance detected during routine testing.
Product
Morphine 50 mg in 0.9% Sodium Chloride 5 mL PCA, 50 mL Cartridge, Concentration: 1 mg/mL, This is a compounded injectable drug; Rx only; Hospital/office use only. SSM St. Clare Outsourcing Facility, Fenton, MO. --- NDC: 88887-6795-01
Category
Drug
Distribution
1 state
ModerateFDA (Devices)·Z-0290-2018·2018-01-03
Remel Shigella sonnei Agglutinating Serum Recalled for Failure to Agglutinate
Remel Inc is recalling Shigella sonnei Agglutinating Serum because it may fail to agglutinate within the specified minimum reaction time.
Product
Remel Shigella sonnei Phase 1 & 2 Agglutinating Serum, Ref R30164201 ZH01. Product Usage: Suitable for the use in slide agglutination tests to identify Shigella cultures presumptively for epidemiological and diagnostic purposes.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0145-2018·2018-01-03
SSM St. Clare Recalls Succinylcholine Chloride Syringes Due to Sterility Concerns
SSM St. Clare Health Center is recalling specific lots of compounded succinylcholine chloride syringes because microbial growth was detected during a routine manufacturing simulation.
Product
Succinylcholine chloride 100 mg in 5 mL syringe, Concentration: 20 mg/mL. This is a compounded injectable drug; Rx only; Hospital/office use only. SSM St. Clare Outsourcing Facility, Fenton, MO --- NDC: 88890-7536-01
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0139-2018·2018-01-03
SSM St. Clare Recalls Hydromorphone PCA Cartridges Due to Sterility Concerns
SSM St. Clare Health Center is recalling specific lots of compounded Hydromorphone PCA cartridges due to a lack of sterility assurance. No distributed product has been confirmed to contain microorganisms.
Product
HYDROmorphone 10 mg in 0.9% Sodium Chloride 50 mL PCA, 50 mL Cartridge, Concentration: 0.2 mg/mL., This is a compounded injectable drug; Rx only; Hospital/office use only. SSM St. Clare Outsourcing Facility, Fenton, MO. --- NDC: 88883-0600-01
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0136-2018·2018-01-03
SSM St. Clare Recalls Fentanyl Vials Due to Sterility Assurance Concerns
SSM St. Clare Health Center is recalling Fentanyl 10 mcg vials because microbial growth was detected during a routine manufacturing simulation. No distributed product has been identified as containing microorganisms.
Product
Fentanyl 10 mcg in 0.9% Sodium Chloride 1 mL, 1 mL Vial, Concentration: 10 mcg/mL, This is a compounded injectable drug; Rx only; Hospital/office use only. SSM St. Clare Outsourcing Facility, Fenton, MO. --- NDC: 88890-9010-81
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0137-2018·2018-01-03
SSM St. Clare Recalls Amiodarone Injectable Due to Sterility Concerns
SSM St. Clare Health Center is recalling a specific lot of compounded Amiodarone injectable bags due to a lack of sterility assurance. No distributed product has been confirmed to contain microorganisms.
Product
Amiodarone 900 mg in dextrose 5% 500 mL, 500 mL bag, Concentration: 1.8 mg/mL, This is a compounded injectable drug; Rx only; Hospital/office use only. SSM St. Clare Outsourcing Facility, Fenton, MO. --- NDC: 88890-0333-01
Category
Drug
Distribution
1 state
LowFDA (Drugs)·D-0130-2018·2018-01-03
Pharmedium Recalls Morphine Sulfate Injection Due to Labeling Errors
Pharmedium Services LLC is recalling morphine sulfate injection due to incorrect or missing lot and expiration dates on the labels.
Product
morphine Sulfate in 0.9% Sodium Chloride Injection 2 mL Total Volume 1 mg per mL (2 mg per 2 mL), For IV Use, Rx Only, Compounded by: PharMEDium Services LLC. 913 N Davis Ave Cleveland, MS 38732, NDC# 61553-259-28
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0132-2018·2018-01-03
Pharmedium Recalls Hydromorphone Injection Due to Labeling Errors
Pharmedium Services LLC is recalling Hydromorphone HCl Injection due to incorrect or missing lot and expiration dates.
Product
HYDROmorphone HCl in 0.9% Sodium Chloride Injection, 1 mL Total Volume 1 mg per mL, For IV Use Only, Rx Only, Compounded by: PharMEDium Services LLC. 913 N Davis Ave Cleveland, MS 38732, NDC# 61553-165-78
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0131-2018·2018-01-03
Pharmedium Recalls Morphine Sulfate Injection Due to Labeling Errors
Pharmedium Services LLC is recalling specific lots of compounded morphine sulfate injection because the labels may have incorrect or missing lot and expiration dates.
Product
morphine Sulfate in 0.9% Sodium Chloride Injection 1 mL Total Volume 2 mg per mL , For IV Use, Rx Only, Compounded by: PharMEDium Services LLC. 913 N Davis Ave Cleveland, MS 38732, NDC# 61553-455-78
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0133-2018·2018-01-03
Auryxia Ferric Citrate Tablets Recalled for Damaged Desiccant Packets
Keryx Biopharmaceuticals is recalling Auryxia (ferric citrate) tablets because damaged silica gel packets may allow desiccant granules to contact the medication.
Product
AURYXIA — AURYXIA (FERRIC CITRATE)
Category
Drug
Distribution
Distributed nationwide
CriticalNHTSA·18E003000·2018-01-02
Takata Frontal Passenger Air Bag Inflator Recall for 2009 Vehicles
Takata is recalling specific 2009 model year air bag inflators that may explode due to propellant degradation. This affects vehicles registered in 22 specific states.
Product
AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
CriticalNHTSA·18E002000·2018-01-02
Takata Frontal Passenger Air Bag Inflator Recall for 2010 Vehicles
Takata is recalling specific frontal passenger air bag inflators in 2010 vehicles registered in 22 states and D.C. due to a risk of explosion causing serious injury or death.
Product
AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V002000·2018-01-02
Forest River Recalls 2018 Surveyor Trailers Due to Fire Risk
Forest River is recalling 2018 Surveyor recreational trailers because an incorrect circuit breaker can cause wiring to melt, increasing the risk of a fire.
Product
FOREST RIVER — FOREST RIVER SURVEYOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18E001000·2018-01-02
Takata Frontal Passenger Air Bag Inflator Recall for 2013 Vehicles
Takata is recalling specific 2013 model year air bag inflators in 13 states and territories due to a risk of explosion from propellant degradation.
Product
AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·18076·2018-01-02
Comfort Research Recalls Ultra Lounge Bean Bag Chair Covers
Comfort Research is recalling about 1,200 Ultra Lounge bean bag chair covers due to risks of entrapment and suffocation to children.
Product
Ultra Lounge bean bag chair covers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·18V001000·2018-01-02
Erwin Hymer Recalls Motorhomes With Defective Fire Extinguishers
Erwin Hymer is recalling 2012-2018 motorhomes because the installed fire extinguishers may clog and fail to discharge properly.
Product
ROADTREK — ROADTREK, CARADO, SUNLIGHT ZION, RS ADVENTUROUS, BANFF, AXION
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·17V847000·2017-12-29
ShowHauler Recalls 2003-2018 Motorhomes Due to Fire Extinguisher Defect
ShowHauler is recalling 2003-2018 Garage Coach, Toter Coach, and Motorhome vehicles because their fire extinguishers may clog or detach, posing injury risks during a fire.
Product
SHOWHAULER — SHOWHAULER GARAGE COACH, TOTER COACH, MOTORHOME
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V845000·2017-12-28
Volvo Bus 9700 Recall: Loose Power Cable Hardware May Cause Overheating
Volvo is recalling 2016-2018 9700 buses because loose hardware on the power supply cable may cause the fuse box to overheat, increasing fire risk.
Product
VOLVO BUS — VOLVO BUS 9700
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V846000·2017-12-28
Forest River Recalls 2017-2018 Georgetown RVs for Brake Defect
Forest River is recalling 2017-2018 Georgetown recreational vehicles because missing plugs in the brake system may cause fluid leaks or air ingestion, increasing stopping distance.
Product
FOREST RIVER — FOREST RIVER GEORGETOWN
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·18712·2017-12-28
Land of Nod Recalls Nook Toddler Beds Due to Entrapment Hazard
Land of Nod is recalling Nook toddler beds because the headboard can disconnect and fall, posing an entrapment risk to children.
Product
Nook toddler beds
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·18073·2017-12-28
Western Gas Recalls Propane Due to Fire and Burn Hazards
Western Gas is recalling under-odorized propane gas due to fire, explosion, and burn hazards. Consumers should contact their supplier for a free inspection.
Product
Propane (LP) Gas
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0122-2018·2017-12-27
LaBri's Body Health XPLODE Recalled for Unapproved Sibutramine
EZWeightLossTX LLC is recalling LaBri's Body Health XPLODE capsules because they contain sibutramine, an unapproved drug ingredient.
Product
LaBri's Body Health XPLODE 30 capsules Exclusively distribute worldwide by LaBri's Body Health.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0115-2018·2017-12-27
Advanced Pharma Recalls Subpotent Nitroglycerin Injection Syringes
Advanced Pharma Inc. is recalling Nitroglycerin injection syringes found to be subpotent, meaning they contain less active ingredient than labeled.
Product
NitroGlycerin (2 mg/10 mL in 5% Dextrose Inj, USP QS 10mL (200 mcg per mL), 10 mL Sterile single dose syringe, packaged in 5 x 5 (TWENTY FIVE) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-863-61.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0121-2018·2017-12-27
FDA Recalls LaBri's Body Health Atomic 60 Capsules for Sibutramine Contamination
EZWeightLossTX LLC is recalling LaBri's Body Health Atomic 60 Capsules because the product was found to contain sibutramine, an unapproved drug ingredient.
Product
LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by LaBri's Body Health.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0123-2018·2017-12-27
Pfizer Recalls Vancomycin Hydrochloride Vials Due to Glass Particulate Matter
Pfizer Inc. is recalling 102,500 vials of Vancomycin Hydrochloride for Injection due to the presence of glass particulate matter.
Product
VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide