The Recall Desk

State

Missouri product recalls

73,598 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
1,339
Severe
2,203
Most recent
2026-10-14

Of the 8,496 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 2,203 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,496 recalls whose distribution notice names Missouri specifically. The 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28201–28225 of 82094

  • HighFDA (Devices)·Z-1157-2021·2021-03-10

    BioFire Film Array BCID Panels Recalled for False Positive Risk

    BioFire Diagnostics is recalling Film Array BCID Panels due to an increased risk of false positive Pseudomonas aeruginosa results when used with specific BD BACTEC vials.

    Product
    Gram-Negative Bacteria And Associated Resistance Markers; Film Array Blood Culture Identification (BCID); Film Array BCID Panel - Product Usage: intended for use with FilmArray systems. Part No: RFIT-ASY-0126 / UDI: 00815381020086 Part No: RFIT-ASY-0127 / UDI: 00815381020093…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V152000·2021-03-10

    Daimler Recalls 2019-2020 Sprinter Vans for Brake Pedal Bolt Issue

    Daimler Vans USA is recalling 2019-2020 Mercedes-Benz and Freightliner Sprinter vans because a brake pedal bolt may detach, causing brake lights to stay on and increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 1500, SPRINTER 2500, SPRINTER 3500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1160-2021·2021-03-10

    United Imaging X-ray System Recalled for Uncommanded Motion Hazard

    Shanghai United Imaging Healthcare is recalling six X-ray systems because the tube head may move unexpectedly, posing a collision risk to patients.

    Product
    Digitial Medica X-ray Imagining System, Model: uDR 596i, RX, CE0123, UDI:(01) 06971576833023 - Product Usage: intended to used by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0327-2021·2021-03-10

    Shenandoah Growers Organic Fresh Cut Basil Recalled for Cyclospora Contamination

    Shenandoah Growers is recalling organic fresh cut basil due to possible contamination with Cyclospora. Consumers should check their pantries for affected products.

    Product
    Organic fresh cut basil packaged in plastic clamshell containers. Shenandoah Growers by Thats Tasty, 0.75 oz UPC: 7-68573-00101-4 Shenandoah Growers by Thats Tasty, 2.0 oz UPC: 7-68573-02143-2 Shenandoah Growers by Thats Tasty 4.0 oz UPC: 7-68573-00141-0 Shenandoah Growers by…
    Category
    Food
    Distribution
    10 states
  • HighNHTSA·21V157000·2021-03-10

    2021 Porsche vehicles recalled for potentially loose suspension components

    Porsche is recalling certain 2021 Taycan, 911, Cayman, Boxster, and 718 Spyder models because suspension components may not have been properly tightened and could loosen, potentially causing loss of vehicle control.

    Product
    PORSCHE — PORSCHE TAYCAN, redundant CAYMAN, redundant BOXSTER, 911
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V153000·2021-03-10

    Mercedes-Benz Sprinter Recalled for Sliding Door Lock Defect

    Daimler Vans USA is recalling 2019-2020 Mercedes-Benz Sprinter vans with optional electric sliding doors because the auxiliary lock may be the incorrect type, potentially increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 1500, SPRINTER 2500, SPRINTER 4500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E018000·2021-03-10

    Safety Belt Solutions Recalls Seat Belts Due to Heat-Treatment Defect

    Safety Belt Solutions is recalling specific seat belts because the tongues may not have been heat-treated correctly, potentially failing to restrain occupants in a crash.

    Product
    SEAT BELTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V159000·2021-03-10

    Audi passenger air bag may not deploy correctly in certain model years

    Volkswagen Group (Audi) is recalling certain 2019-2021 Audi models for defective passenger air bags that may not deploy properly during a crash. Owners should contact Audi at 1-800-253-2834 for free inspection and repair.

    Product
    AUDI — AUDI A6, A7, A6 ALLROAD, S6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1158-2021·2021-03-10

    BioFire BCID2 Panel Recalled for False Positive Pseudomonas Results

    BioFire Diagnostics is recalling BCID2 Panels due to a risk of false positive Pseudomonas aeruginosa results when used with specific BD BACTEC blood culture vials.

    Product
    BioFire BCID2 Panel; IVD, Rx Only Part No: RFIT-ASY-0147 / UDI: 00815381020338 - Product Usage: intended for use with FilmArray systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1151-2021·2021-03-10

    Baxter Recalls PrisMax Hemodialysis Tubing Due to Performance Variability

    Baxter Healthcare is recalling PrisMax System Version II hemodialysis tubing due to performance variability that may cause alarms and therapy interruptions.

    Product
    The PrisMax System Version II Hemodialysis Delivery System: Automatic Repositioning System Pump Assembly, specifically tubing, Model Numbers: a) 955626 b) 955558 c) 955701 PrisMax V2 Preventive Maintenance Kit, Product Code SC616 ARPS PUMP, Product Code SC6035 ARPS Pump…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V156000·2021-03-10

    2021 BMW XB7, X5, and X7 Head Restraints May Detach in Crash

    BMW is recalling certain 2021 XB7, X5, and X7 vehicles because the head restraints on second-row outer seats may be an incorrect type and could detach during a crash, increasing injury risk.

    Product
    BMW — BMW X7, XB7, X5, X5 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21092·2021-03-10

    Lifetime Products Recalls 6-Foot Seminar Tables Due to Injury Risk

    Lifetime Products is recalling 6-foot seminar tables because the brace arms may fail to lock, causing the table to collapse and posing an injury risk.

    Product
    Lifetime Products 6-foot Seminar Tables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21093·2021-03-10

    Hillsdale Jennings Counter and Bar Stools Recalled for Fall Hazard

    Hillsdale Furniture is recalling Jennings counter and bar stools because the seat can break off the base, posing a fall hazard.

    Product
    Hillsdale Furniture Jennings Counter and Bar Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V161000·2021-03-10

    2019-2021 Genesis G70 Engine Compartment Fire Risk from ABS Module

    Hyundai is recalling 2019-2021 Genesis G70 vehicles because the Anti-Lock Brake System module could short-circuit and cause an engine compartment fire. Owners should park outside until the ABS module fuse is replaced.

    Product
    GENESIS — GENESIS G70
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1173-2021·2021-03-10

    Siemens Sensis Vibe Systems Recalled for Potential System Freezes

    Siemens is recalling 37 Sensis Vibe systems in the US because they may sporadically freeze during operation or idle, preventing user interaction.

    Product
    Sensis / Sensis Vibe systems with software version VD12 and equipped with HP Flex Pro-C PC. Diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies Model Numbers: Sensis Vibe Hemo 11007641 Sensis Vibe Combo 11007642 Sensis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0296-2021·2021-03-10

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the delivery system is out of specification for mechanical peel.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1153-2021·2021-03-10

    Bovie Velocity Disposable Bipolar Ablators Recalled for Sterile Packaging Defect

    Bovie Medical Corporation is recalling Velocity Disposable Bipolar Ablators because pinholes in the sterile packaging may compromise the sterile barrier.

    Product
    Velocity Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1170-2021·2021-03-10

    Boston Scientific Recalls Polypectomy Snares Due to Incomplete Pouch Seals

    Boston Scientific is recalling Captivator, Captiflex, and Sensation polypectomy snares because users reported incomplete pouch seals before use.

    Product
    Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares Outer box UPN, Inner pouch UPN: M00560311 (Box 5), M00560310; M00560321 (Box 5), M00560320; M00562651 (Box 5), M00562650; M00562652 (Box 20), M00562650; M00562671 (Box 5), M00562670…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0293-2021·2021-03-10

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling 473,280 Daytrana (methylphenidate) patches because the delivery system failed mechanical peel specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0295-2021·2021-03-10

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling 786,900 Daytrana (methylphenidate) patches because the delivery system failed mechanical peel specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1155-2021·2021-03-10

    Bovie Medical Recalls ConMed Disposable Bipolar Ablators Due to Packaging Defect

    Bovie Medical Corporation is recalling 5,270 ConMed Disposable Bipolar Ablators because pinholes in the sterile packaging may compromise the sterile barrier.

    Product
    ConMed Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0292-2021·2021-03-10

    Dr. Reddy's Recalls Progesterone Capsules Due to Dissolution Failures

    Dr. Reddy's Laboratories is recalling 16,449 bottles of 200 mg Progesterone Capsules because stability testing revealed out-of-specification dissolution results.

    Product
    PROGESTERONE — PROGESTERONE (PROGESTERONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1164-2021·2021-03-10

    G & H Wire Company Recalls Orthodontic Elastic Bands Due to Labeling Error

    G & H Wire Company is recalling orthodontic elastic bands because the patient pack text is incorrect, which could lead to misuse and temporary discomfort.

    Product
    Band, Elastic, Orthodontic - Product Usage: Orthodontic elastics, also referred to as rubber bands, are small stretchy loops of rubber that help move teeth into proper alignment during orthodontic treatment. Their purpose is to create additional force for tooth movement in any…
    Category
    Medical Device
    Distribution
    Distributed nationwide