The Recall Desk

State

Missouri product recalls

20,307 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.

12551–12575 of 20307

  • SevereFDA (Devices)·Z-1952-2023·2023-07-05

    FDA Recalls Teleflex Endotracheal Tubes for Connector Disconnection

    The FDA is recalling approximately 302,652 Teleflex preformed oral endotracheal tubes nationwide due to reports of disconnection between the 15mm connector and the tube. Healthcare providers should immediately discontinue use of affected units.

    Product
    Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1956-2023·2023-07-05

    Preformed AGT Oral Endotracheal Tubes Recalled for Connector Disconnection

    Teleflex is recalling 35,513 preformed AGT oral endotracheal tubes nationwide due to reported connector disconnection from the 15mm tube connector.

    Product
    Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781070
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1860-2023·2023-07-05

    Endotracheal Tube Connector Disconnection Recall

    TELEFLEX LLC is recalling Slick Set Cuffed Endotracheal Tubes (REF 1700100) due to reports of the 15mm connector disconnecting from the device during use.

    Product
    Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 1700100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1891-2023·2023-07-05

    Teleflex Endotracheal Tubes Recalled for 15mm Connector Disconnection

    Teleflex is recalling approximately 39,550 endotracheal tubes due to reports of 15mm connector disconnection. The FDA Class I recall affects units distributed nationwide including Puerto Rico.

    Product
    Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082085
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1959-2023·2023-07-05

    Endotracheal Tubes Recalled for Potential 15mm Connector Disconnection

    TELEFLEX is recalling 4,160 endotracheal tubes due to reports of the 15mm connector disconnecting from the tube. Affected units were distributed nationwide.

    Product
    Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1954-2023·2023-07-05

    Preformed AGT Endotracheal Tubes Recalled for Connector Disconnection Risk

    TELEFLEX is recalling approximately 43,571 units of Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection from the tube, affecting nationwide distribution including Puerto Rico.

    Product
    Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1846-2023·2023-07-05

    Endotracheal Tube Connector Disconnection Risk in Flexi-Set Kit

    Flexi-Set Cuffed Endotracheal Tube kits are being recalled due to reports of the 15mm connector disconnecting from the tube. Affected units were distributed nationwide.

    Product
    Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504555
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1832-2023·2023-07-05

    Slick Set Endotracheal Tubes Recalled for Connector Disconnection Risk

    Teleflex is recalling Slick Set Cuffed Endotracheal Tubes due to reports of the 15mm connector disconnecting from the tube, which could interrupt airway support during mechanical ventilation.

    Product
    Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170075
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1951-2023·2023-07-05

    Endotracheal Tube Connector Disconnection Recalled by Teleflex

    Teleflex recalls 76,060 preformed oral endotracheal tubes due to reports of 15mm connector disconnection. A disconnected connector could compromise ventilation in critical care settings.

    Product
    Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781035
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1845-2023·2023-07-05

    Flexi-Set Cuffed Endotracheal Tube Recall: Connector Disconnection Risk

    Teleflex is recalling Flexi-Set Cuffed Endotracheal Tubes due to reports of 15mm connector disconnection. The recall affects 66,310 units distributed nationwide.

    Product
    Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504550
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1932-2023·2023-07-05

    Teleflex Endotracheal Tubes: FDA Recalls 1110 Units for Connector Disconnection

    Teleflex is recalling 1,110 endotracheal tubes due to reports of 15mm connector disconnection. The affected units are distributed nationwide in the US and Puerto Rico.

    Product
    Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1943-2023·2023-07-05

    Oral Endotracheal Tubes Recalled for 15mm Connector Disconnection Risk

    Teleflex LLC is recalling 19,842 preformed oral endotracheal tubes due to reports of 15mm connector disconnection. Affected devices were distributed nationwide.

    Product
    Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1883-2023·2023-07-05

    Endotracheal Tube Connector Disconnection Risk Prompts FDA Class I Recall

    TELEFLEX LLC is recalling 690 endotracheal tubes with high-volume, low-pressure cuff due to reports of connector disconnection. The affected products were distributed nationwide.

    Product
    Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1960-2023·2023-07-05

    Endotracheal Tubes Recalled Due to 15mm Connector Disconnection Reports

    TELEFLEX LLC is recalling 6,710 endotracheal tubes due to reports of 15mm connector disconnection. This Class I recall affects units distributed nationwide.

    Product
    Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080065
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1905-2023·2023-07-05

    Slick Set Endotracheal Tubes Recalled for Connector Disconnection Risk

    Teleflex is recalling Slick Set Uncuffed Endotracheal Tubes due to reports of disconnection of the 15mm connector. The affected products have been distributed nationwide including Puerto Rico.

    Product
    Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150055
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1996-2023·2023-07-05

    MEGADYNE MEGA SOFT Patient Return Electrode Recalled for Reported Patient Burns

    Megadyne Medical Products is recalling the MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode used in electrosurgery due to reports of patient burns during surgical procedures.

    Product
    MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode. used during electrosurgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1862-2023·2023-07-05

    Preformed AGT Endotracheal Tubes Recalled for Connector Disconnection Risk

    Teleflex is recalling 4,769 endotracheal tubes due to reports of 15mm connector disconnection. This defect could interrupt breathing support during airway management procedures.

    Product
    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180035
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1857-2023·2023-07-05

    Flexi-Set Uncuffed Endotracheal Tubes recalled for connector disconnection risk

    TELEFLEX LLC recalls Flexi-Set Uncuffed Endotracheal Tube and Stylet Sets due to reports of the 15mm connector disconnecting from the tube. Approximately 16,400 units distributed nationwide are affected.

    Product
    Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506540
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V355000·2023-07-05

    2022 International CV Vehicles Brake Sensor Fitting May Cause Brake Failure

    Navistar is recalling certain 2022 International CV vehicles because the pressure sensor fitting on the brake line assembly may not be tightened correctly, potentially causing brake fluid loss and brake failure.

    Product
    INTERNATIONAL — 2022 INTERNATIONAL CV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1896-2023·2023-07-05

    Tracheal tube connector disconnection reported in RUSCHELIT Safety Clear models

    TELEFLEX LLC is recalling RUSCHELIT Safety Clear Tracheal Tubes due to reports of 15mm connector disconnection. The recall involves 21,284 units distributed nationwide.

    Product
    RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480030
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1925-2023·2023-07-05

    Endotracheal Tube Connector Disconnection Reported by Teleflex

    Teleflex is recalling endotracheal tubes due to reports of disconnection between the tube and its 15mm connector. Affected devices were distributed nationwide including Puerto Rico.

    Product
    Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380025
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1855-2023·2023-07-05

    Teleflex Flexi-Set Endotracheal Tubes Recalled for Connector Disconnection

    Teleflex is recalling 32,553 units of Flexi-Set Uncuffed Endotracheal Tubes nationwide due to reports of 15mm connector disconnections that could compromise airway management.

    Product
    Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506530
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1849-2023·2023-07-05

    Flexi-Set Endotracheal Tubes recalled for connector disconnection

    Teleflex is recalling over 1 million Flexi-Set Cuffed Endotracheal Tube kits due to reports of 15mm connector disconnection from the tube. The recall affects products distributed nationwide.

    Product
    Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504570
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1865-2023·2023-07-05

    Preformed Endotracheal Tubes Recalled for Connector Disconnection

    Teleflex is recalling 4,146 preformed endotracheal tubes due to reports of 15mm connector disconnection. The affected devices were distributed nationwide.

    Product
    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1998-2023·2023-07-05

    Patient Return Electrode Recalled Due to Burn Reports During Surgery

    Megadyne Medical Products is recalling MEGA SOFT Universal Patient Return Electrodes after reports of patient burns during electrosurgery procedures. The FDA classified this as a Class I recall.

    Product
    MEGADYNE MEGA SOFT Universal Patient Return Electrode. used during electrosurgery
    Category
    Medical Device
    Distribution
    Distributed nationwide