The Recall Desk

State

Missouri product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53701–53725 of 82334

  • SevereFDA (Food)·F-1575-2016·2016-07-06

    Reser's Potato Salad Recalled for Potential Listeria Contamination

    Reser's Fine Foods is recalling refrigerated potato salad products due to potential Listeria monocytogenes contamination from a recalled onion lot.

    Product
    Reser's Original Potato Salad, Refrigerated, Retail package, Net wt. 3.5 oz. UPC 0 71117 17000 9. Reser's Original Potato Salad, Refrigerated, Retail package, Net wt. 5.5 oz. UPC 0 71117 17100 6. Reser's Original Potato Salad, Refrigerated, Retail package, Net wt. 8…
    Category
    Food
    Distribution
    30 states
  • SevereCPSC·16214·2016-07-06

    Overstock Recalls Self-Balancing Scooters Due to Fire Hazard

    Overstock.com is recalling about 4,300 self-balancing scooters sold online from September to December 2015 because their lithium-ion batteries can overheat and catch fire.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1578-2016·2016-07-06

    Safeway Classic Potato Salad Recalled for Listeria Contamination Risk

    Reser's Fine Foods is recalling Safeway Classic Potato Salad due to potential Listeria monocytogenes contamination from a recalled onion lot.

    Product
    Safeway Classic Potato Salad, Refrigerated, Retail package, net wt. 5.5oz. UPC 0 21130 06716 9.
    Category
    Food
    Distribution
    30 states
  • SevereCPSC·16211·2016-07-06

    Swagway Recalls Self-Balancing Scooters Due to Fire and Explosion Hazards

    Swagway is recalling X1 hoverboards because their lithium-ion batteries can overheat, smoke, catch fire, or explode. Consumers should stop using the units and contact Swagway for a repair or credit.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·16218·2016-07-06

    Ten Firms Recall Self-Balancing Scooters Due to Fire and Explosion Hazards

    Ten companies are recalling about 501,000 self-balancing scooters because their lithium-ion batteries can overheat, catch fire, or explode. Consumers should stop using these products immediately.

    Product
    Self-Balancing Scooters/Hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1577-2016·2016-07-06

    Stonemill Kitchens Potato Salad Recalled for Listeria Risk

    Reser's Fine Foods is recalling Stonemill Kitchens Classic Potato Salad due to potential Listeria monocytogenes contamination from a recalled onion lot.

    Product
    Stonemill Kitchens Classic Potato Salad, Refrigerated, Retail net wt. 5lb. UPC 0 71117 61576 0.
    Category
    Food
    Distribution
    30 states
  • SevereFDA (Food)·F-1580-2016·2016-07-06

    Reser's Potato Salad Recalled for Potential Listeria Contamination

    Reser's Fine Foods is recalling Walmart Redskin Potato Salad due to potential Listeria monocytogenes contamination from a recalled onion lot.

    Product
    Walmart Redskin Potato Salad, Refrigerated, Retail net wt. 4lb. UPC 81131 91693 6.
    Category
    Food
    Distribution
    30 states
  • SevereFDA (Devices)·Z-2060-2016·2016-07-06

    Hospira Recalls PlumSet IV Administration Sets Due to Fluid Leakage

    Hospira is recalling PlumSet IV administration sets because intravenous fluid may leak at the secondary port. The recall covers 3,920,932 units distributed in the US and Canada.

    Product
    *** 1) Product labeled in part: List No. 14220-28; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, CLAVE Y-Site, Non-Vented, 110 Inch, Non-DEHP; Product Usage: The CLAVE of the secondary port is used as an easy secondary access that allows concurrent and piggyback mode…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V512000·2016-07-06

    Newmar Recalls 2017 Motorhomes Due to Front Fascia Wood Trim Separation Risk

    Newmar is recalling 152 model year 2017 motorhomes because front fascia wood trim may separate and contact occupants, potentially causing loss of vehicle control.

    Product
    NEWMAR — NEWMAR DUTCH STAR, KING AIRE, MOUNTAIN AIRE, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16216·2016-07-06

    Keenford Recalls iMoto Hoverboards Due to Fire and Explosion Risks

    Keenford Limited is recalling about 84,000 iMoto self-balancing scooters because their lithium-ion batteries can overheat, smoke, catch fire, or explode.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2064-2016·2016-07-06

    CareFusion Alaris System PC Unit Recall for Incorrect Patient Weight Data

    CareFusion 303, Inc. is recalling 69,693 Alaris System PC Units because the RESTORE feature may incorrectly populate patient weight for specific infusion modules.

    Product
    Alaris System PC Unit Model 8015 with software versions 9.17 and 9.19; Central programming, monitoring and power supply component for the Alaris System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2053-2016·2016-07-06

    Nephron Recalls Sodium Chloride Inhalation Solution Due to Sterility Concerns

    Nephron Pharmaceuticals is recalling 11,208 cartons of Sodium Chloride Inhalation Solution because internal dye tests failed to confirm vial integrity.

    Product
    Sodium Chloride Inhalation Solution, USP 3%, 60 x 4 mL Sterile Unit-Dose Vials per carton, Rx Only, NDC 0487-9003-60. A vial contains sterile, preservation-free, clear, colorless, aqueous solution as labeled for induction of sputum production where specimen collection is…
    Category
    Medical Device
    Distribution
    36 states
  • HighFDA (Devices)·Z-2056-2016·2016-07-06

    Hospira Symbiq Infusion Pumps Recalled for False Occlusion Alarms

    Hospira is recalling Symbiq Two Channel Infusers due to frequent false occlusion alarms that may delay or interrupt patient therapy.

    Product
    Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids Device is a general purpose infusion pump designed to deliver fluids, solutions, medications, agents, nutritionals, electrolytes, blood and blood products for parenteral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16217·2016-07-06

    Hype Wireless Recalls Self-Balancing Scooters Due to Fire Hazard

    Hype Wireless is recalling about 25,000 Roam brand self-balancing scooters because their lithium-ion batteries can overheat, posing a risk of smoking, fire, or explosion.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2092-2016·2016-07-06

    Smith & Nephew Legion Hinge Knee Femoral Assembly Recall

    Smith & Nephew is recalling Legion Hinge Knee femoral assemblies because the cement application surface is below specification.

    Product
    LEGION(TM) HK FEMORAL ASSEMBLY, SIZE 4 LEFT, A/P 58.5 MM, M/L 66 MM, REF 71421374 The LEGION Hinge Knee System is indicated for: 1. Rheumatoid arthritis. 2. Post-traumatic arthritis, osteoarthritis, or degenerative arthritis in older patients whose age, weight and activity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2104-2016·2016-07-06

    Medical Depot Recalls Aluminum Crutches Due to Tip Failure

    Medical Depot Inc. is recalling 123,125 pairs of Universal Quick Adjust aluminum crutches because the metal tips may fail and detach from the ground.

    Product
    Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, tall adult, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16208·2016-07-06

    PTX Performance Products Recalls Airwalk Hoverboards Due to Fire Hazard

    PTX Performance Products is recalling about 4,900 Airwalk self-balancing scooters because the lithium-ion batteries can overheat, posing a risk of fire or explosion.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2062-2016·2016-07-06

    Hospira Recalls LifeShield IV Sets Due to Potential Fluid Leakage

    Hospira is recalling approximately 3.9 million LifeShield IV administration sets because fluid may leak at the secondary port.

    Product
    *** 1) Product labeled in part: 19683-28; LIFESHIELD; MICRODRIP SOLUSET WITH 1.2 MICRON FILTER 150ML BURETTE PLUMSET, CONVERTIBLE PIN, CLAVE SECONDARY PORT, OPTION-LOK, NON-DEHP; NOMINAL LENGTH: 118 IN; PRIMING VOLUME: 14 ML; *** 2) Product labeled in part: List No. 19685-28…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16209·2016-07-06

    Yuka Clothing Recalls Self-Balancing Scooters Due to Fire Hazard

    Yuka Clothing is recalling about 800 self-balancing scooters sold nationwide and online because the lithium-ion battery packs can overheat, posing a risk of smoking, fire, or explosion.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2054-2016·2016-07-06

    Nephron Recalls Sodium Chloride Inhalation Solution Due to Sterility Concerns

    Nephron Pharmaceuticals is recalling 13,692 cartons of Sodium Chloride Inhalation Solution due to a failure in the internal dye ingress test, which raises concerns about the sterility of the vials.

    Product
    Sodium Chloride Inhalation Solution, USP 7%, 60 x 4 mL Sterile Unit-Dose Vials, Rx Only, NDC 0487-9007-60. A vial contains sterile, preservation-free, clear, colorless, aqueous solution as labeled for induction of sputum production where specimen collection is indicated. For…
    Category
    Medical Device
    Distribution
    36 states
  • HighFDA (Devices)·Z-2049-2016·2016-07-06

    Baxter Recalls PrismaSate Dialysis Solution Bags Due to Leaks

    Baxter Healthcare is recalling 10,054 units of PrismaSate BGK2/0 Dialysis Solution for Continuous Renal Replacement Therapy because of leaks near the top of the bags.

    Product
    PrismaSate BGK2/0 Dialysis Solution for Continuous Renal Replacement Therapy
    Category
    Medical Device
    Distribution
    32 states
  • HighCPSC·16756·2016-07-06

    Little Lotus Baby Swaddles and Sleeping Bags Recalled for Choking Hazard

    Embrace Technologies is recalling Little Lotus baby swaddles and sleeping bags because shoulder snaps can break or detach, posing a choking hazard to young children.

    Product
    Little Lotus baby swaddles and sleeping bags
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2087-2016·2016-07-06

    Siemens Hettich Centrifuge Modules Recalled for Premature Bucket Failures

    Siemens Healthcare Diagnostics Inc. is recalling 487 Hettich Centrifuge Modules due to premature bucket failures. The units were distributed nationwide.

    Product
    Hettich Centrifuge Modules: StreamLAB Centrifuge Module (10372372 or 10444807 or 10706836) Aptio Centrifuge Module (10703032 or 10713761) FlexLab High Throughput Centrifuge Module (11171747) FlexLab and Aptio Centrifuge Module (10628157 or 11266581): Used to separate…
    Category
    Medical Device
    Distribution
    Distributed nationwide