The Recall Desk

State

Colorado product recalls

20,322 recalls have nationwide distribution and so reach Colorado. 0 additional recalls listed Colorado specifically in their distribution scope.

About recalls in Colorado

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 Colorado 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.

12576–12600 of 20322

  • 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-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-1924-2023·2023-07-05

    Teleflex Endotracheal Tubes Recalled for 15mm Connector Disconnection

    Teleflex is recalling Preformed AGT Oral Endotracheal Tubes due to reports of the 15mm connector disconnecting from the tube. Approximately 2,980 units were distributed nationwide.

    Product
    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181065
    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-1895-2023·2023-07-05

    RUSCHELIT Safety Clear Tracheal Tubes recalled for connector disconnection risk

    Teleflex is recalling RUSCHELIT Safety Clear Tracheal Tubes due to reports of 15mm connector disconnection. The affected tubes are distributed nationwide.

    Product
    RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480025
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1839-2023·2023-07-05

    Endotracheal Tube Connector Disconnection Risk Prompts Teleflex Recall

    Teleflex is recalling Slick Set Uncuffed Endotracheal Tubes due to reported 15mm connector disconnection. The recall affects 22,400 units distributed nationwide.

    Product
    Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170130
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1837-2023·2023-07-05

    Slick Set Endotracheal Tubes recalled due to reported 15mm connector disconnection

    Teleflex is recalling Slick Set Uncuffed Endotracheal Tubes due to reports of the 15mm connector disconnecting from the tube. The recall affects 14,160 units distributed nationwide.

    Product
    Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170120
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1836-2023·2023-07-05

    Teleflex Slick Set Endotracheal Tube Connector May Disconnect

    Teleflex recalled 720 units of its Slick Set Cuffed Endotracheal Tube and Stylet Set due to reports of connector disconnection. The recall affects units distributed nationwide including Puerto Rico.

    Product
    Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170095
    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-1827-2023·2023-07-05

    Endotracheal Tube and Stylet Set Connector May Disconnect During Use

    TELEFLEX is recalling Slick Set Cuffed Endotracheal Tube and Stylet Sets due to reports that the 15mm connector may disconnect from the tube during use.

    Product
    Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1934-2023·2023-07-05

    Endotracheal Tubes With 15mm Connector Disconnection Recalled Nationwide

    TELEFLEX is recalling 25,630 endotracheal tubes nationwide because the 15mm connector can disconnect. The affected products were distributed throughout the United States and Puerto Rico.

    Product
    Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382025
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1923-2023·2023-07-05

    Teleflex Endotracheal Tubes Recalled Due to Connector Disconnection Risk

    Teleflex is recalling 8,610 Preformed AGT Oral Endotracheal Tubes nationwide due to reports that the 15mm connector can disconnect from the tube.

    Product
    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1886-2023·2023-07-05

    Teleflex Endotracheal Tubes Recalled for Connector Disconnection Risk

    Teleflex is recalling approximately 170,610 endotracheal tubes due to reports of 15mm connector disconnection. The disconnection could compromise airway management during mechanical ventilation.

    Product
    Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1937-2023·2023-07-05

    Teleflex Endotracheal Tubes Recalled Due to Connector Disconnection

    Teleflex LLC is recalling 7,800 endotracheal tubes due to reports of the 15mm connector disconnecting from the tube. The affected products were distributed nationwide in the US and Puerto Rico.

    Product
    Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382055
    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-1995-2023·2023-07-05

    MEGADYNE MEGA SOFT Reusable Patient Return Electrode Recalled for Patient Burn Hazard

    Megadyne Medical Products is recalling 21,100 MEGADYNE MEGA SOFT Reusable Patient Return Electrodes nationwide due to reports of patient burns during electrosurgical procedures.

    Product
    MEGADYNE MEGA SOFT Reusable Patient Return Electrode. used during electrosurgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1875-2023·2023-07-05

    Endotracheal Tubes Recalled for 15mm Connector Disconnection

    TELEFLEX is recalling approximately 25,435 endotracheal tubes (REF 100382035) distributed nationwide due to reported disconnection of the 15mm connector from the device.

    Product
    Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382035
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1861-2023·2023-07-05

    Preformed Endotracheal Tube Connector Disconnection Recall by TELEFLEX

    TELEFLEX LLC is recalling 3,100 preformed oral endotracheal tubes nationwide due to reports of 15mm connector disconnection that could compromise airway management.

    Product
    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180030
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1940-2023·2023-07-05

    Endotracheal Tube 15mm Connector Disconnection Recall

    Teleflex is recalling endotracheal tubes after reports that the 15mm connector may disconnect from the tube. The recall affects 36,135 units distributed nationwide.

    Product
    Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780035
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1900-2023·2023-07-05

    FDA Recalls Slick Set Uncuffed Endotracheal Tubes for Connector Disconnection

    Teleflex is recalling approximately 2,550 Slick Set Uncuffed Endotracheal Tubes (REF 150020) due to reports of 15mm connector disconnection.

    Product
    Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150020
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1894-2023·2023-07-05

    Endotracheal tubes recalled for 15mm connector disconnection

    Teleflex is recalling 19,250 endotracheal tubes because the 15mm connector may disconnect during use, potentially compromising airway management in patients.

    Product
    Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2001-2023·2023-07-05

    Megadyne Mega Soft Universal Patient Return Electrode Recalled for Burn Risk

    Megadyne Medical Products is recalling 21,100 MEGA SOFT electrosurgery patient return electrodes distributed nationwide due to reports of patient burns during surgical procedures.

    Product
    MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode. used during electrosurgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1958-2023·2023-07-05

    Teleflex Endotracheal Tubes Recalled Due to Connector Disconnection Risk

    Teleflex endotracheal tubes are recalled nationwide due to reported disconnection of the 15mm connector. The recall affects 1,750 units distributed across the US and Puerto Rico.

    Product
    Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1871-2023·2023-07-05

    Preformed AGT Endotracheal Tubes Recalled for Connector Disconnection Risk

    Teleflex is recalling 12,852 units of Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection from the tube. Affected units were distributed nationwide including Puerto Rico.

    Product
    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181040
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1843-2023·2023-07-05

    Slick Set Endotracheal Tubes Recalled for Connector Disconnection

    Teleflex LLC is recalling Slick Set Endotracheal Tube Sets for reports of 15mm connector disconnection. The connector may separate from the tube, affecting respiratory support in patients.

    Product
    Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170150
    Category
    Medical Device
    Distribution
    Distributed nationwide