The Recall Desk

State

Massachusetts product recalls

20,307 recalls have nationwide distribution and so reach Massachusetts. 0 additional recalls listed Massachusetts specifically in their distribution scope.

About recalls in Massachusetts

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 Massachusetts 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.

12626–12650 of 20307

  • 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-1848-2023·2023-07-05

    Endotracheal Tube Sets Recalled for Connector Disconnection Risk

    Teleflex is recalling Flexi-Set Cuffed Endotracheal Tube Sets due to reported 15mm connector disconnection. The recall affects 92,930 units distributed throughout the United States, including Puerto Rico.

    Product
    Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504565
    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-1856-2023·2023-07-05

    Flexi-Set Endotracheal Tube Recalled for Connector Disconnection

    Teleflex is recalling 18,353 Flexi-Set Uncuffed Endotracheal Tube sets nationwide due to reports of 15mm connector disconnection. The defect could affect ventilation during use.

    Product
    Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506535
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1939-2023·2023-07-05

    Endotracheal Tubes Recalled for Connector Disconnection by Teleflex

    TELEFLEX LLC is recalling 2,140 endotracheal tubes nationwide due to reports of the 15mm connector disconnecting from the tube. Affected units were distributed throughout the United States, including Puerto Rico.

    Product
    Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382065
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1904-2023·2023-07-05

    Endotracheal Tube Connector Disconnection Risk Prompts Medical Device Recall

    Teleflex is recalling Slick Set Uncuffed Endotracheal Tube and Stylet Sets due to reports that the 15mm connector may disconnect from the tube. The recall affects 447 units distributed nationwide.

    Product
    Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150040
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1953-2023·2023-07-05

    Endotracheal Tubes Recalled for Potential 15mm Connector Disconnection

    TELEFLEX LLC is recalling Preformed AGT Oral Endotracheal Tubes because the 15mm connector may disconnect from the tube, creating a potential airway access risk.

    Product
    Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781055
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1926-2023·2023-07-05

    TELEFLEX Endotracheal Tubes Recalled for 15mm Connector Disconnection

    TELEFLEX is recalling 5,990 endotracheal tubes due to reports of 15mm connector disconnection. Affected units were distributed nationwide, including Puerto Rico.

    Product
    Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380030
    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-1901-2023·2023-07-05

    Slick Set Endotracheal Tubes recalled for connector disconnection

    TELEFLEX is recalling 2,382 Slick Set Uncuffed Endotracheal Tubes due to reports of 15mm connector disconnection. Units were distributed nationwide including Puerto Rico.

    Product
    Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150025
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1844-2023·2023-07-05

    Slick Set Uncuffed Endotracheal Tube Connector Disconnection Risk

    TELEFLEX is recalling 3,310 units of Slick Set Uncuffed Endotracheal Tubes (REF 170155) distributed nationwide due to reports of the 15mm connector disconnecting from the tube.

    Product
    Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170155
    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-1854-2023·2023-07-05

    Flexi-Set Endotracheal Tubes Recalled for 15mm Connector Disconnection

    Teleflex is recalling 17,551 units of Flexi-Set Uncuffed Endotracheal Tubes nationwide after reports of the 15mm connector disconnecting from the tube.

    Product
    Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506525
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1840-2023·2023-07-05

    Endotracheal Tube Connector Disconnection Hazard in Teleflex Slick Set

    Teleflex is recalling Slick Set Uncuffed Endotracheal Tube kits due to reports of 15mm connector disconnection. 20,662 units have been distributed nationwide, including Puerto Rico.

    Product
    Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170135
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1880-2023·2023-07-05

    Endotracheal Tubes Recalled Due to Connector Disconnection Risk

    Teleflex LLC is recalling 17,840 Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection. These tubes have been distributed nationwide including Puerto Rico.

    Product
    Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781075
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1830-2023·2023-07-05

    Slick Set endotracheal tubes recalled for connector disconnection

    Teleflex is recalling Slick Set endotracheal tubes due to reports of 15mm connector disconnection. The defect could prevent proper airway management during patient care.

    Product
    Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170065
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1850-2023·2023-07-05

    Flexi-Set Endotracheal Tube Connectors Recalled Due to Disconnection Risk

    TELEFLEX LLC is recalling Flexi-Set Cuffed Endotracheal Tube and Stylet Sets due to reports of 15mm connector disconnection. Approximately 684,042 units were distributed nationwide, including Puerto Rico.

    Product
    Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504575
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1965-2023·2023-07-05

    Teleflex Endotracheal Tube Recalled for Connector Disconnection Risk

    Teleflex LLC is recalling 670 endotracheal tubes due to reports that the 15mm connector is disconnecting from the tube. Affected units were distributed nationwide including Puerto Rico.

    Product
    Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080090
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1938-2023·2023-07-05

    TELEFLEX Endotracheal Tubes Recalled for 15mm Connector Disconnection

    TELEFLEX is recalling 5,600 endotracheal tubes nationwide due to reports of 15mm connector disconnection that could compromise airway management during patient care.

    Product
    Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1847-2023·2023-07-05

    Flexi-Set Endotracheal Tubes recalled for connector disconnection risk

    TELEFLEX LLC is recalling Flexi-Set Cuffed Endotracheal Tube and Stylet Sets nationwide due to reports of connector disconnection. The affected devices may disconnect during use, potentially compromising airway management.

    Product
    Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504560
    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-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-1957-2023·2023-07-05

    Preformed AGT Oral Endotracheal Tubes Recalled for Connector Disconnection

    TELEFLEX is recalling approximately 8,620 Preformed AGT Oral Endotracheal Tubes distributed nationwide due to reports of disconnection of the 15mm connector from the tube.

    Product
    Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781080
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1936-2023·2023-07-05

    Endotracheal Tubes Recalled for Connector Disconnection Risk

    Teleflex LLC is recalling 11,188 endotracheal tubes due to reports of 15mm connector disconnection. The defect affects this critical airway management device nationwide.

    Product
    Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382045
    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