The Recall Desk

State

Missouri product recalls

20,322 recalls have nationwide distribution and so reach Missouri. 0 additional recalls listed Missouri specifically in their distribution scope.

About recalls in Missouri

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Missouri consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

13076–13100 of 20322

  • HighNHTSA·22V263000·2023-06-04

    Tesla Model 3 Speedometer Unit Display May Fail in Track Mode

    Tesla is recalling certain 2018-2022 Model 3 Performance vehicles because the speedometer's mph/km/h unit display may fail in Track Mode. Drivers may not know their vehicle's speed, increasing crash risk. Tesla will provide a free software update.

    Product
    TESLA — 2020 TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V252000·2023-06-04

    2022–2023 Land Rover Range Rover Seat Frame Defect Recall

    Jaguar Land Rover North America is recalling certain 2022–2023 Land Rover Range Rover vehicles because the second-row left seat frame may have been insufficiently welded and may not adequately secure occupants during crashes or sudden braking.

    Product
    LAND ROVER — 2022 LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V306000·2023-06-04

    Tiffin Bus and Phaeton motorhomes recalled for fuel rail leakage and fire risk

    Tiffin Motorhomes is recalling 2017-2021 Bus and Phaeton vehicles due to fuel rail assembly defects that may leak, posing a fire risk. Owners should contact Tiffin customer service at 1-256-356-8661 for a free inspection.

    Product
    TIFFIN — 2021 TIFFIN BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V146000·2023-06-03

    2023 Triumph Bonneville T120 motorcycles recalled for brake disc detachment risk

    Triumph is recalling certain 2023 Bonneville T120 motorcycles because the left-hand side brake disc may detach, reducing brake performance and increasing crash risk. Dealers will install replacement parts free of charge.

    Product
    TRIUMPH — 2023 TRIUMPH BONNEVILLE T120
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V223000·2023-06-03

    2020-2021 Lincoln Aviator vehicles recalled for backup camera display failure

    Ford is recalling 2020-2021 Lincoln Aviator vehicles because the backup camera display may not show video feed, affecting rear visibility. Free software updates are available from Ford dealers.

    Product
    LINCOLN — 2020 LINCOLN AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V221000·2023-06-03

    2021 Alfa Romeo Stelvio Side Curtain Air Bag May Fail to Deploy

    2021 Alfa Romeo Stelvio vehicles may have improperly crimped clamps in the side curtain air bag assembly, which can fail to deploy in a crash, increasing injury risk. Chrysler will replace the assemblies at no cost.

    Product
    ALFA ROMEO — 2021 ALFA ROMEO STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23212·2023-06-01

    EGO Power+ Cordless Hedge Trimmers recalled for unexpected activation and laceration risk

    Chervon North America is recalling about 85,000 EGO Power+ Model HT2410 Cordless Brushless Hedge Trimmers due to a faulty rear trigger switch. The company has received 34 reports of unexpected activation, including 8 that caused lacerations requiring stitches.

    Product
    EGO Power+ Model HT2410 Cordless Brushless Hedge Trimmers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23213·2023-06-01

    PowerXL Self-Cleaning Juicers recalled for laceration and ingestion hazards

    Empower Brands is recalling about 469,000 PowerXL Self-Cleaning Juicers because they can rupture during use, causing cuts, or leave particle shavings in juice. The company is aware of 261 incident reports including 47 injuries.

    Product
    PowerXL Self-Cleaning Juicers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V016000·2023-06-01

    2022 Peterbilt 579 chassis step bolts may loosen and cause injury

    Bolts securing the chassis fairing step assembly on certain 2022 Peterbilt 579 vehicles may loosen and fracture. This can cause the step to move unexpectedly while entering or exiting the cab, increasing the risk of injury.

    Product
    PETERBILT — 2022 PETERBILT 579
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·23211·2023-06-01

    Jetson Nova and Star 3-Wheel Kick Scooters Recalled for Fall Hazard

    Jetson Electric Bikes is recalling about 15,300 Nova and Star 3-Wheel Kick Scooters because the rear wheel can loosen or fall off, posing a fall hazard to children. The company has received 12 reports of wheel loosening or falling, including one injury.

    Product
    Jetson Nova and Star 3-Wheel Kick Scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1594-2023·2023-05-31

    COVID-19 At-Home Test Kits Recalled for Bacterial Buffer Contamination

    SD Biosensor is recalling 2,712,767 Pilot COVID-19 At-Home Test kits nationwide due to bacterial contamination in the liquid buffer component. Users may notice an odor from affected kits.

    Product
    Pilot COVID-19 At-Home Test, Reference Number 9901-NCOV-10G, Catalog Number 99COV200L-EN02, UPC Code: 887473000207 (EAN-13: 08800111707728)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0650-2023·2023-05-31

    Cardioplegia Solution Nationwide Recall Due to Sterility Assurance Failure

    Central Admixture Pharmacy Services is recalling 255 bags of Cardioplegia Solution after FDA inspection questioned its sterility assurance. The product was distributed nationwide.

    Product
    Cardioplegia Solution, Reperfusate No Potassium, packaged in 238.75 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0005-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0679-2023·2023-05-31

    Cardioplegia Solution Recalled Due to Sterility Assurance Failure

    Central Admixture Pharmacy Services recalls Cardioplegia Solution (325 bags nationwide) after FDA inspection identified loss of sterility assurance. Product is used in cardiac surgery and requires prescription.

    Product
    Cardioplegia Solution, Maintenance 8:1 non-enriched, low potassium, 24 mEq K, packaged in 300 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0215-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0706-2023·2023-05-31

    Injectable oxyTOCIN and Lactated Ringer's Recalled Over Sterility Concerns

    Central Admixture Pharmacy Services is recalling oxyTOCIN with Lactated Ringer's injection (14,362 bags) nationwide due to FDA inspection findings that questioned sterility assurance.

    Product
    oxyTOCIN 20 units added to Lactated Ringer's 1,000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6038-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0738-2023·2023-05-31

    FDA Recalls Diphenhydramine Injectable for Sterility Assurance Deficiency

    Central Admixture Pharmacy Services is recalling 3,999 units of diphenhydramine injectable due to sterility assurance concerns identified during an FDA inspection. No illnesses have been reported.

    Product
    diphenhydrAMINE 50 mg added to 0.9% sodium chloride 50 mL in 100 mL Partial Additive Bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7090-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0727-2023·2023-05-31

    FDA Recalls Phenylephrine Injectable Due to Sterility Concerns

    Central Admixture Pharmacy Services is recalling 5,304 bags of phenylephrine injection nationwide after FDA inspection raised concerns about product sterility assurance.

    Product
    PHENYLephrine added to 0.9% sodium chloride, 25 mg/250 mL* (100 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7011-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0690-2023·2023-05-31

    Neonatal TPN Starter Bags Recalled Over Sterility Assurance Failure

    Central Admixture Pharmacy Services is recalling 418 bags of neonatal TPN starter bags nationwide due to loss of sterility assurance following FDA inspection. The prescription product contains amino acids, dextrose, calcium, and heparin.

    Product
    Neonatal TPN Starter Bag, Amino Acids (Trophamine) 3%/Dextrose 5% with CALCIUM and HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0419-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0758-2023·2023-05-31

    Glimepiride Tablets recalled due to manufacturing practice deviations

    Amerisource Health Services is recalling 105,361 bottles of Glimepiride Tablets nationwide following FDA discovery of manufacturing practice deviations. No illnesses have been reported.

    Product
    Glimepiride Tablets, USP, 2 mg, RX, Packaged as a ) 100-count bottle, NDC# 68001-178-00; b) 500-count bottle; NDC# 68001-178-03 Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213, INDIA. For BluePoint Laboratories
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0732-2023·2023-05-31

    FDA Recalls Heparin Injectable Due to Sterility Assurance Failure

    Central Admixture Pharmacy Services is recalling 5,207 bags of heparin injectable nationwide due to an FDA-identified sterility assurance failure. The company cannot guarantee the sterility of affected lot numbers.

    Product
    heparin added to 0.9% sodium chloride, 5,000 units/500 mL* (10 units/mL), 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7023-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0667-2023·2023-05-31

    Cardioplegia Solution Recalled Due to Sterility Concerns

    Central Admixture Pharmacy Services is recalling 476 bags of Cardioplegia Solution nationwide because an FDA inspection raised concerns about the product's sterile assurance.

    Product
    Cardioplegia Solution, Maintenance 4:1 Plasma-Lyte/Tromethamine, low potassium, packaged in 1000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0112-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0734-2023·2023-05-31

    NORepinephrine Injectable Recalled Nationwide for Sterility Assurance Failure

    Central Admixture Pharmacy Services is recalling 6,341 bags of NORepinephrine nationwide due to FDA concerns about sterility assurance. An FDA inspection found the manufacturer could not adequately ensure the product's sterility.

    Product
    NORepinephrine added to 0.9% sodium chloride, 16 mg/250 mL* (64 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7036-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0656-2023·2023-05-31

    FDA Recalls Microplegia Solution for Sterility Assurance Concerns

    Central Admixture Pharmacy Services recalls Microplegia Solution due to sterility assurance concerns identified during an FDA inspection. Affected product should not be used.

    Product
    Microplegia Solution, MSA/MSG 0.92 Molar with CP2D, packaged in 120 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0012-2.
    Category
    Drug
    Distribution
    Distributed nationwide