The Recall Desk

State

Missouri product recalls

73,734 recalls have nationwide distribution and so reach Missouri. 8,500 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,500
Critical
1,339
Severe
2,203
Most recent
2026-10-28

Of the 8,500 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 8,500 recalls whose distribution notice names Missouri specifically. The 73,734 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30051–30075 of 82234

  • HighFDA (Devices)·Z-0091-2021·2020-10-21

    Mizuho OSI Recalls Levo Arms Due to Fluid Ingress Risk

    Mizuho OSI is recalling 174 Levo Arms used in spinal surgery tables due to a potential fluid ingress issue that could cause the locking mechanism to fail.

    Product
    Levo Arm Label: LEVO ARM REF 7887-050 MIZUHO OSI Refurbished Levo Arm Label: LEVO ARM REF 7887-050R MIZUHO OSI - Product Usage: used with Mizuho OSI spinal surgery tables to provide patient head support and positioning during spinal surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0109-2021·2020-10-21

    SkyVision SDS System Recalled for Intermittent Video Signal Failure

    Skytron is recalling 36 SkyVision SDS System units because intermittent signal failures can cause monitors to go blank during surgery, increasing patient risk.

    Product
    SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product Usage: is a high quality, self-contained video switching and control unit for use in the operating room.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0023-2021·2020-10-21

    Lucky Spoon Bakery Recalls Gluten-Free Brownie Bites Due to Gluten Contamination

    Lucky Spoon Bakery is recalling specific lots of Gluten Free Chewy Chocolatey Brownie Bites because a flour supplier's batch tested positive for gluten.

    Product
    Lucky Spoon Bakery Gluten Free Chewy Chocolatey Brownie Bites, 6.6 oz. plastic clam shell containing approximately 12 (6.6 oz.), UPC 8-50489-00315-9, P.O. Box 2954 Salt Lake City, UT 84110. 12 packages/case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0020-2021·2020-10-21

    Lucky Spoon Bakery Recalls Gluten-Free Cupcakes Due to Gluten Contamination

    Lucky Spoon Bakery is recalling gluten-free cupcakes because a flour batch tested positive for gluten. The products were distributed in eight states and nationwide via drop ship.

    Product
    Lucky Spoon Bakery Gluten Free Very Vanilla Cupcakes with Vanilla Buttercream Frosting, 8.0 oz. plastic clam shell containing 4 cupcakes, UPC 8-50489-00309-8, P.O. Box 2954 Salt Lake City, UT 84110. 12 packages/case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0019-2021·2020-10-21

    Lucky Spoon Bakery Recalls Gluten-Free Muffins Due to Gluten Contamination

    Lucky Spoon Bakery is recalling Gluten Free Utterly Almond Muffins because a flour supplier's batch tested positive for gluten.

    Product
    Lucky Spoon Bakery Gluten Free Utterly Almond Muffins, 7.25 oz. plastic clam shell containing 6 muffins, UPC 8-50489-00305-0, P.O. Box 2954, Salt Lake City, UT 84110. 12 packages/case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·20V647000·2020-10-21

    Braun Ambulances Recall 156 Units Due to Display Lockup

    Braun Ambulances is recalling 156 units because the lighting and HVAC display may lock up, potentially delaying emergency operations and increasing crash risk.

    Product
    BRAUN AMBULANCES — BRAUN AMBULANCES EXPRESS PLUS TYPE I, CHIEF XL TYPE III, LIBERTY TYPE I, EXPRESS TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0095-2021·2020-10-21

    Alcon Custom-Pak Surgical Packs Recalled for Latex Glove Degradation

    Alcon is recalling 16,971 Custom-Pak Surgical Procedure Packs containing Cardinal Health PROTEXIS Latex Micro Surgical Gloves due to a degradation defect that could cause holes or tears.

    Product
    Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health" PROTEXIS" Latex Micro Surgical Gloves - Product Usage: used by ophthalmic surgeons in a variety of ophthalmic surgeries.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0097-2021·2020-10-21

    Biomet Recalls RingLoc Hip Cups Due to Double Sterilization

    Biomet is recalling 48 RingLoc Bi-Polar Hip System Acetabular Cups because they were gamma sterilized twice, which may compromise functionality and shelf life.

    Product
    (1) RingLoc Bi-Polar Hip System Acetabular Cup ArCom: Acetabular Bi-Polar Cup, E1 Antioxidant Infused, 28 MM, 41 MM: Item No. 110010458; Lot No. 710930; UDI No. (01) 00880304568747 (17) 230614 (10) 710930 (2) RingLoc Hip system Acetabular Bi-Polar Cup: Acetabular Cup…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0092-2021·2020-10-21

    Getinge Servo-i Ventilator Recall for Short Nebulizer Connector

    Getinge is recalling 431 Servo-i Ventilators because a nebulizer connector may be shorter than specified, potentially preventing the Aeroneb Nebulizer module from installing successfully.

    Product
    Servo-i Ventilator, Part No. 6487800, UDI Code 07325710000823 - Product Usage: intended for general and critical ventilator care, and it can be used for low end to high end intensive care, in different configurations. It supports a variety of breathing modes and can be used for…
    Category
    Medical Device
    Distribution
    15 states
  • ModerateFDA (Devices)·Z-0105-2021·2020-10-21

    Cook Inc. Recalls Percutaneous Neonatal Pigtail Nephrostomy Sets

    Cook Inc. is recalling 368 Percutaneous Neonatal Pigtail Nephrostomy Sets because the indwell time is decreasing from 4 months to 4 weeks.

    Product
    Percutaneous Neonatal Pigtail Nephrostomy Set, Reference Part Number 080106, Order Number G14508. The set contains a 22 gage, 5 cm Chiba Needle; an 18 gage, 5 cm trocar needle; an .038-inch (.97 mm) diameter, 30 cm PTFE-coated stainless steel; a 5, 6, and 7 French, 10 cm…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0107-2021·2020-10-21

    Ezycare Disposable Face Masks Recalled for Mislabeling as Non-Medical

    FDA is recalling Ezycare disposable face masks because they were labeled as non-medical but distributed to customers expecting medical use.

    Product
    Ezycare Face Mask, Disposable Non Medical Face Masks - Product Usage: marketed under face mask umbrella EUA as source control.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0093-2021·2020-10-21

    Biomet Shoulder Prosthesis Baseplate Packaging Error Recall

    Biomet is recalling 3 units of Comprehensive Reverse Shoulder Glenosphere Mini Baseplates due to packaging errors where components may be missing or duplicated.

    Product
    Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate with Taper Adapter-Shoulder Prosthesis item: 010000589 - Product Usage: intended to serve as the foundation for the reverse shoulder prosthesis head (glenosphere).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0106-2021·2020-10-21

    Cook Inc. Recalls Pediatric Nephrostomy Stent Sets Due to Labeling Update

    Cook Inc. is recalling 380 Pediatric Nephrostomy Stent Sets because the indwell time is decreasing from 4 months to 4 weeks. The Instructions for Use are being updated to reflect this change.

    Product
    Pediatric Nephrostomy Stent Set, Reference Part Numbers 080208-S6 and 080208-S7, Order Numbers G15034 and G15035. The set contains a radiopaque pigtail catheter and stent, retention disc with pull tie, and a 10 French, 30 cm polyvinylchloride connecting tube with one-way…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0104-2021·2020-10-21

    Roche Recalls Albumin Gen.2 Reagents Due to Cross-Contamination

    Roche Diagnostics is recalling Albumin Gen.2 reagents due to cross-contamination causing low quality recovery and invalid calibrations.

    Product
    Albumin Gen.2, Catalog 05166861190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0103-2021·2020-10-21

    Roche Recalls Tina-quant Complement C4 Reagents Due to Quality Issues

    Roche Diagnostics is recalling 180 units of Tina-quant Complement C4 reagents due to cross-contamination causing invalid calibrations.

    Product
    Tina-quant Complement C4 ver.2, Catalog 05991994190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V646000·2020-10-19

    Mitsubishi Fuso Trucks Recalled for Loose Exhaust Studs and Fire Risk

    Mitsubishi Fuso is recalling 2019-2021 FEC7T, FEC9T, and FECZT trucks because loose exhaust studs may allow hot gases to leak, increasing fire risk.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO FEC7T, FEC9T, FECZT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V645000·2020-10-19

    Mitsubishi Fuso Trucks Recalled for Brake Booster Vacuum Pump Defect

    Mitsubishi Fuso is recalling 2019-2021 FEC7T, FEC9T, and FECZT trucks because heat from the exhaust manifold may crack the brake booster vacuum pump diaphragm, potentially disabling power brake assist.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO FEC7T, FEC9T, FECZT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V644000·2020-10-19

    Audi Recalls One 2020 Q3 for Driver's Seat Frame Bolt Defect

    Audi is recalling one 2020 Q3 because the driver's seat frame may be incorrectly bolted to the seat rail, increasing injury risk in a crash.

    Product
    AUDI — AUDI Q3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E079000·2020-10-17

    Fuel Delivery Module Recall Due to Potential Stalling Risk

    Continental Automotive Systems is recalling Vitesco NG2 Fuel Delivery Modules where a plastic burr may block the mixing tube, causing insufficient fuel supply and vehicle stalling.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E078000·2020-10-16

    Weldon V-Mux Vista IV LCD Displays Recalled for Electrical Lockup

    Akron Brass is recalling Weldon V-Mux Vista IV LCD displays used in emergency vehicles because they may lock up due to voltage spikes, potentially delaying emergency efforts.

    Product
    ELECTRICAL SYSTEM: INSTRUMENT CLUSTER/PANEL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide