The Recall Desk

State

Missouri product recalls

20,199 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.

9776–9800 of 20199

  • HighFDA (Devices)·Z-1341-2024·2024-03-27

    Angiodynamics Guidewire Introducer Recall Due to Manufacturing Defect

    Angiodynamics recalls approximately 5,840 guidewire introducers with manufacturing defects that may prevent proper guidewire insertion during vascular procedures. The defect could cause procedural delays requiring equipment exchange.

    Product
    MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-759
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1314-2024·2024-03-27

    Abbott Point of Care Control Device Recalled Due to Temperature Storage Failure

    Abbott's i-STAT Level 1 control device is recalled because a refrigerator temperature excursion on January 8, 2024, could cause incorrect or delayed test results. The walk-in storage unit failed, causing temperatures to fall below the required range of 35.6-46.4°F.

    Product
    Abbott Point of Care Control Control i-STAT¿ Level 1 10 X 1.7 mL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1331-2024·2024-03-27

    Directional Laser Probe Recalled for Fiber Extension and Direction Difficulties

    D.O.R.C. Dutch Ophthalmic Research Center is recalling Directional Laser Probes for ophthalmic surgery due to difficulties extending, retracting, and directing the laser fiber. The recall affects 84 units distributed nationwide.

    Product
    Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0389-2024·2024-03-27

    Digoxin Tablets Recalled Due to Cross Contamination with Mycophenolate Mofetil

    Novitium Pharma LLC recalls Digoxin 125mcg tablets nationwide due to cross contamination with mycophenolate mofetil, a different medication. Patients receiving contaminated tablets could experience unintended drug effects.

    Product
    DIGOXIN — DIGOXIN (DIGOXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1350-2024·2024-03-27

    Convatec EsteemBody Drainable Pouches Recalled for Filter Weld Defect

    ConvaTec is recalling specific lots of EsteemBody Soft Convex Drainable Pouches due to inconsistency in filter weld strength, affecting 6709 units distributed in the US and internationally.

    Product
    Convatec EsteemBody Soft Convex, Drainable Pouch, Product codes (REF): a) 423643, b) 423658, c) 423659, d) 423664, e) 423666, f) 423645, g) 423667, h) 423657, i) 423652, j) 423646, k) 423654, l) 423653, m) 423647, n) 423644, o) 423648, p) 423665, q) 423656, r) 423651, s) 423660,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1330-2024·2024-03-27

    Laparotomy Sponges recalled for incomplete sterilization and missing RF detection

    Covidien is recalling Situate Laparotomy Sponges because some packs may contain improperly sterilized units lacking required RF detection features. Non-sterile sponges could cause infection, tissue trauma, and sepsis during surgery.

    Product
    Situate Laparotomy Sponge, RF and X-ray Detectable, REF: L1818-04P01C-1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1348-2024·2024-03-27

    Guidewire Introducer Sheath Recalled for Internal Lumen Voids

    Angiodynamics is recalling 39 units of MINI STICK MAX vascular guidewire introducers due to voids in the sheath hub that may prevent guidewire passage during surgery, potentially delaying the procedure.

    Product
    MINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. - Catalog Number: 45-781
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1335-2024·2024-03-27

    Angiodynamics Guidewire Introducer Devices Recalled for Manufacturing Defects

    Angiodynamics recalls MINI STICK MAX guidewire introducer devices due to manufacturing defects in the internal lumen that may prevent guidewire passage and delay surgical procedures.

    Product
    MINI STICK MAX 4F X 10 CM STD .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-750
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1346-2024·2024-03-27

    Guidewire Introducer Sheath from Angiodynamics Recalled for Manufacturing Defect

    Angiodynamics is recalling 65 units of its MINI STICK MAX guidewire introducer sheath due to manufacturing defects that may prevent guidewires from passing through during surgical procedures.

    Product
    MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-775
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1305-2024·2024-03-27

    Conductive Adhesive Gel Recalled Due to Thickness and Discoloration Issues

    Natus Neurology is recalling TENSIVE Conductive Adhesive Gel (Lot A0623009) after complaints of improper thickness, discoloration, and in one case, patient skin irritation following use.

    Product
    TENSIVE Conductive Adhesive Gel, REF 016-401600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1311-2024·2024-03-27

    Sekisui OSOM BVBLUE Bacterial Vaginosis Control Kit recalled due to temperature exposure

    A Sekisui Diagnostics control kit for bacterial vaginosis testing was recalled after exposure to temperatures below the validated storage range for up to 60 minutes due to refrigerator mechanical failure.

    Product
    Sekisui Diagnostics Control Kit OSOM¿ BVBLUE¿ Bacterial Vaginosis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1313-2024·2024-03-27

    Steris Endo Cleaning Indicator Recalled Due to Temperature Excursion

    Mckesson Medical-Surgical is recalling Steris Endo Cleaning Indicator VERIFY RESITEST devices due to temperature excursions that occurred on January 8, 2024. The temperature drop could cause the indicator to produce incorrect or delayed test results.

    Product
    Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1344-2024·2024-03-27

    Guidewire Introducer Sheath with Manufacturing Defect Recalled by Angiodynamics

    Angiodynamics is recalling MINI STICK MAX guidewire introducer sheaths due to manufacturing defects that may prevent guidewire passage. The defect may cause procedural delays requiring equipment exchange during vascular interventions.

    Product
    MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-767
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1349-2024·2024-03-27

    Landauer microStar Reader dosimetry system discontinued for medical applications

    Landauer is permanently discontinuing the microStar Reader medical dosimetry system. The company is removing product documentation references and discontinuing use with medical dosimeters.

    Product
    microStar Reader, Model Numbers: 10015-000 (marketed in EMEA as 100, 102, 110, and 201), 10016-000 (marketed in EMEA as 101), 10036-000, 10044-000, 10055-000, BC30058, and BC30059
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1338-2024·2024-03-27

    Vascular Guidewire Introducer Sheath Recall Due to Manufacturing Defect

    Angiodynamics is recalling certain MINI STICK MAX vascular guidewire introducer sheaths due to internal voids that may prevent guidewire passage during surgery, potentially causing procedural delays.

    Product
    MINI STICK MAX 5F X 10 CM STD .018 SS/SS ECHO 2.75" PG -Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-754
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1336-2024·2024-03-27

    FDA Recalls Vascular Guidewire Introducer Due to Manufacturing Defect

    Angiodynamics is recalling 959 units of MINI STICK MAX guidewire introducers due to voids in the sheath hub that may prevent proper guidewire placement. Users may experience procedure delays and need to exchange equipment.

    Product
    MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-751
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1306-2024·2024-03-27

    Natus Sleep Supplies Recalled for Conductive Adhesive Gel Quality Defects

    Natus Neurology is recalling Sleep Supplies Start Kits due to defective conductive adhesive gel supplied by Parker Laboratories. The gel is too thick, discolored, and caused patient irritation in at least one case.

    Product
    natus neurology, Sleep Supplies Start Kit with Single Use Supplies for Embla EX Series Amplifiers, REF 024252
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1339-2024·2024-03-27

    Angiodynamics surgical guidewire recalled for manufacturing defect

    Angiodynamics is recalling 5,176 units of MINI STICK MAX guidewires due to manufacturing voids that prevent passage through the introducer during surgery. Surgeons may need to exchange the sheath to complete procedures.

    Product
    MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 2.75" PG Catalog Number: 45-756
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1315-2024·2024-03-27

    Laboratory Control Material Recalled Due to Temperature Storage Excursion

    Abbott Point of Care Control i-STAT Level 3 control material (Lot 121164) is being recalled due to temperature excursions in storage that could affect test accuracy. Affected units were distributed in Arizona, Pennsylvania, and Texas.

    Product
    Abbott Point of Care Control Control i-STAT¿ Level 3 1.7 mL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalCPSC·24169·2024-03-21

    Happiness USA Roller Ball Candy Recalled Due to Choking Hazard

    Twenty Four Six Foods LLC is recalling all flavors of Happiness USA Liquid Rolling Candy because the rolling ball applicator can dislodge into a child's mouth, posing a choking hazard and risk of death.

    Product
    Happiness USA Liquid Rolling Candy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24171·2024-03-21

    Starbucks-branded metallic mugs recalled due to burn and laceration hazards

    Nestlé USA recalls about 440,500 metallic mugs from 2023 holiday Starbucks gift sets sold at Target, Walmart, and military retailers. The mugs can overheat or break when microwaved or filled with extremely hot liquid, causing severe burns and cuts. 10 people have been injured in 12 reported incidents.

    Product
    Metallic Mugs included in 2023 Holiday Starbucks-branded Gift Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24172·2024-03-21

    BRS and BULin Liquid Fuel Bottles Recalled for Unsafe Closures

    BRS and BULin portable liquid fuel bottles sold on Amazon have non-child-resistant closures that violate federal safety law, posing risks of burns and poisoning to children. Consumers should stop using them and contact the seller for disposal and refund instructions.

    Product
    BRS and BULin Liquid Fuel Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24174·2024-03-21

    Ravin R500 Series Crossbows Recalled for Unexpected Discharge Injury Risk

    Ravin Crossbows LLC is recalling about 13,300 R500 series crossbows because they can unexpectedly discharge while being cocked or uncocked if not fully cocked, posing an injury hazard. The company has received one report of unexpected discharge but no injuries have been reported.

    Product
    Ravin R500 Model Crossbows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24168·2024-03-21

    Crown Aruba IV Gas Boilers Recalled for Carbon Monoxide Hazard

    Crown Boiler Company is recalling about 1,100 Crown Aruba IV (AWR Series) gas-fired hot water boilers due to a blocked vent switch that can fail to shut down burners at high altitudes, allowing carbon monoxide to accumulate in homes.

    Product
    Crown Aruba IV (AWR Series) gas-fired hot water boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide