The Recall Desk

State

Missouri product recalls

72,907 recalls have nationwide distribution and so reach Missouri. 8,461 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,461
Critical
1,333
Severe
1,870
Most recent
2026-09-09

Of the 8,461 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 1,870 (22%) are Severe.

These figures cover only the 8,461 recalls whose distribution notice names Missouri specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1326–1350 of 81368

  • ModerateFDA (Drugs)·D-0634-2026·2026-06-24

    Cura Hongos clotrimazole cream recalled over manufacturing practice deviations

    Cura Hongos Crema Antifungica, clotrimazole 1%, in 2 oz tubes is being recalled because of CGMP deviations and deficiencies observed during an FDA inspection. 84 tubes affected.

    Product
    Cura Hongos, Crema Antifungica, Clotrimazole 1%, 2oz (57g) tubes, Dist by/por: Pharmadel LLC, New Castle, DE 19720, Made in India, UPC 8 52924 00683 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2444-2026·2026-06-24

    Medline vascular and cardiac packs contain recalled Mastisol liquid adhesive

    Medline convenience kits including AV fistula, endovascular, EP device and aneurysm packs are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: BIB AV FISTULA PACK DYNJ58304B CARDIAC MINOR SURGICOUNT PACK DYNJ56573B ENDOVASCULAR PACK DYNJ29135N EP DEVICE DYNJ65916B FULL LINE ANEURYSM CDS CDS983672P GEN FEM POP #14-RF DYNJ21877W IMPLANT PACK DYNJ39316D OPEN HEART MR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2427-2026·2026-06-24

    Medline hernia repair totes contain recalled Mastisol liquid adhesive

    The Medline Hernia Repair Tote convenience kit is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.

    Product
    Medline convenience kit: HERNIA REPAIR TOTE DYNJ908337D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2436-2026·2026-06-24

    Medline ACDF and ACL procedure kits contain recalled Mastisol adhesive

    Medline convenience kits for ACD, ACDF, ACL and ALIF procedures are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: ACD DYNJ904999J ACDF DYNJ907336B DYNJ910821A ACDF PACK DYNJ81098C ACL DYNJ911996 ACL ACCESSORY PACK DYNJ86584B ACL- LF DYNJ905281B ACL PACK DYNJ67271A ALIF DYNJ904848L ANTERIOR CERVICAL DYNJ901355J ARTHROSCOPY DYN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2434-2026·2026-06-24

    Medline da Vinci main kits contain recalled Mastisol liquid adhesive

    Medline da Vinci Main convenience kits are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.

    Product
    Medline convenience kits: DAVINCI MAIN DYNJ908031D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0592-2026·2026-06-24

    Kerr Insta-Char 50 gram charcoal suspension did not meet OTC monograph

    VistaPharm Kerr Insta-Char, 50 grams activated charcoal in a sorbitol base, is being recalled because the product did not meet Over-the-Counter Monograph M023.

    Product
    VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 50 Grams Activated Charcoal in 52 Grams Sorbitol in 240 mL (8 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-203-08.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0590-2026·2026-06-24

    Kerr Insta-Char aqueous charcoal suspension did not meet OTC monograph

    VistaPharm Kerr Insta-Char in an aqueous base, 50 grams activated charcoal, is being recalled because the product did not meet Over-the-Counter Monograph M023.

    Product
    VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 50 Grams Activated Charcoal in 240 ml (8 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-202-08.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0608-2026·2026-06-24

    Focalin XR 5mg capsules carry incorrect or missing lot and expiry

    Focalin XR 5 mg extended-release capsules are being recalled over a labeling issue: incorrect or missing lot number and/or expiry date. 7,803 bottles are affected.

    Product
    FOCALIN — FOCALIN (DEXMETHYLPHENIDATE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V399000·2026-06-23

    GM Recalls 2025-2026 Savana and Express for Steering Nut Issue

    General Motors is recalling 2025-2026 GMC Savana and Chevrolet Express vehicles because a steering gear nut may be loose, risking loss of control.

    Product
    GMC — GMC, CHEVROLET SAVANA, EXPRESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E037000·2026-06-23

    Rockford Fosgate Amplifier Kits Recalled for Fire Risk

    Rockford Corporation is recalling specific amplifier kits because a fuse may fail to protect against short circuits, increasing the risk of a fire.

    Product
    ELECTRICAL SYSTEM:WIRING:FUSES AND CIRCUIT BREAKERS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26E038000·2026-06-23

    Ricon Recalls S-Series and K-Series Wheelchair Platform Lifts

    Ricon is recalling S-Series and K-Series wheelchair platform lifts because a failed electrical contactor may prevent the controls from stopping the lift.

    Product
    EQUIPMENT ADAPTIVE/MOBILITY:WHEELCHAIR LIFT/RAMP:CONTROLS/CONTROL WIRING recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V400000·2026-06-23

    Hyundai Tucson instrument panel displays may fail due to software error

    Hyundai is recalling certain 2025-2026 Tucson, Tucson Hybrid and Tucson Plug-In Hybrid vehicles because a software error may cause the instrument panel display to fail.

    Product
    HYUNDAI — HYUNDAI TUCSON PLUG-IN HYBRID, TUCSON HYBRID, TUCSON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E036000·2026-06-19

    Airxcel Recalls MaxxAir N-Series Maxxfan Fans Due to Overheating Risk

    Airxcel is recalling MaxxAir N-Series Maxxfan rooftop ventilation fans because the printed circuit board may overheat, increasing the risk of a fire.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V397000·2026-06-19

    Indian Motorcycle Recalls 2026 Chief Vintage for Incorrect Rim Labeling

    Indian Motorcycle is recalling 2026 Chief Vintage models because the VIN label lists the wrong rear rim width, which could lead to improper tire mounting and loss of control.

    Product
    INDIAN — INDIAN CHIEF VINTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26563·2026-06-18

    Arrogantf Spa Drain Covers Recalled Over Entrapment and Drowning Hazards

    Arrogantf spa drain covers sold on Amazon violate federal safety standards and pose entrapment and drowning hazards. Consumers should stop using them immediately and contact the importer for a refund.

    Product
    Arrogantf Spa Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26562·2026-06-18

    GOPO Toys pull string teething toys reported to cause choking incidents

    About 70,410 GOPO Toys pull string teething toys are being recalled after three reports of the silicone strings reaching the back of a child's throat, causing respiratory distress or choking.

    Product
    GOPO TOYS Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26561·2026-06-18

    BABESIDE doll and stroller toy sets violate the small parts ban

    About 2,200 BABESIDE doll and stroller toy sets are being recalled because the small pacifier violates the small parts ban and the plush bear's eyes can detach.

    Product
    BABESIDE Doll and Stroller Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V393000·2026-06-18

    2026 Subaru Solterra battery electric vehicles loss of drive power

    Toyota Motor Engineering & Manufacturing is recalling 2026 Subaru Solterra vehicles due to a fault in the battery electronic control unit that may cause loss of drive power, increasing crash risk.

    Product
    SUBARU — SUBARU, TOYOTA, LEXUS SOLTERRA, BZ, RZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V395000·2026-06-18

    Farber Specialty Recalls 2025-2026 Emergency Vehicles Due to Touchscreen Failure

    Farber Specialty is recalling 2025-2026 HX620 and MCXCR emergency vehicles because the touchscreen may fail, preventing the activation of exterior lights and emergency equipment.

    Product
    FARBER SPECIALTY — FARBER SPECIALTY MCXCR, HX620 SBA 6X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26568·2026-06-18

    Joolz Aer2 car seat adapters can detach, allowing the seat to fall

    About 3,840 Joolz Aer2 Car Seat Adapters are being recalled because they can fail to attach properly to the stroller, which may allow the car seat to fall.

    Product
    Joolz Aer2 Car Seat Adapters for Joolz Aer 2 Stroller
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26564·2026-06-18

    Veseacky Children's Pajama Sets Recalled for Burn Hazard

    Veseacky children's pajama sets are recalled due to burn hazards from violating mandatory safety standards for children's sleepwear. About 3,700 units were sold on Amazon from October 2020 through January 2026.

    Product
    Veseacky Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V394000·2026-06-18

    2026–2027 Cadillac Vistiq Third-Row Seat Power Fold Feature Recall

    General Motors is recalling 2026–2027 Cadillac Vistiq vehicles because the third-row power seatback may fail to reverse when it encounters a person, potentially trapping them.

    Product
    CADILLAC — CADILLAC VISTIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide