The Recall Desk

Severity 4 of 5

Severe recalls

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

2276–2300 of 4878

  • SevereFDA (Food)·F-1299-2023·2023-07-05

    Sun Wave Brand Jelly Cup Recalled for Potential Choking Hazard

    Richin Trading Inc is recalling 141,192 units of Sun Wave Brand Jelly Cup due to a potential choking hazard. Affected products were distributed across 17 US states.

    Product
    Sun Wave Brand Jelly Cup (Assorted Flavors); Made in Taiwan; Item Number 12151; UPC 715685121512; Net Weight 35.27 oz. (1000 g) Sun Wave Brand Jelly Cup (Assorted Flavors); Made in Taiwan; Item Number 12143; UPC 715685121437; Net Weight 52.91 oz. (1500 g)
    Category
    Food
    Distribution
    17 states
  • 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-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-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-1881-2023·2023-07-05

    Endotracheal Tubes Recalled for 15mm Connector Disconnection

    TELEFLEX LLC recalls 2,520 endotracheal tubes (model REF 112080055) due to reports of 15mm connector disconnection. The disconnection could compromise airway function during critical care use.

    Product
    Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080055
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1946-2023·2023-07-05

    Preformed AGT oral endotracheal tube connector disconnection recalled

    Teleflex LLC recalls 14,780 preformed AGT oral endotracheal tubes due to reports of 15mm connector disconnection. Units were distributed nationwide.

    Product
    Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780065
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1899-2023·2023-07-05

    RUSCHELIT Safety Clear Tracheal Tubes Recalled for Connector Disconnection

    TELEFLEX LLC recalls RUSCHELIT Safety Clear Tracheal Tubes due to reports of 15mm connector disconnection. The Class I recall affects 30,391 units distributed nationwide including Puerto Rico.

    Product
    RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480045
    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 (Food)·F-1300-2023·2023-07-05

    Sun Wave Brand Jelly Cups recalled for choking hazard

    Richin Trading Inc is recalling Sun Wave Brand Mango Jelly Cups due to a potential choking hazard. The recall affects 141,192 units distributed across 17 states.

    Product
    Sun Wave Brand Jelly Cup (Mango Flavor); Made in Taiwan; Item Number 12153; UPC 715685121536; Net Weight 35.27 oz. (1000 g) Sun Wave Brand Jelly Cup (Mango Flavor); Made in Taiwan; Item Number 12144; UPC 715685121444; Net Weight 52.91 oz. (1500 g)
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Devices)·Z-1887-2023·2023-07-05

    Endotracheal Tube Connectors May Disconnect - Teleflex Recall

    Teleflex endotracheal tubes with specific batch numbers may experience disconnection of the 15mm connector during clinical use. The FDA has classified this as a Class I recall affecting 247,645 units distributed nationwide.

    Product
    Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082065
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1935-2023·2023-07-05

    Endotracheal Tubes Recalled Due to Connector Disconnection Issues

    Teleflex LLC is recalling 17,102 Endotracheal Tubes (REF 100382040) following reports of disconnection of the 15mm connector from the tube. The affected units were distributed nationwide, including Puerto Rico.

    Product
    Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382040
    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-1944-2023·2023-07-05

    Endotracheal Tube Connector Disconnection Recalls 14,480 Units

    Teleflex is recalling 14,480 Preformed AGT Oral Endotracheal Tubes nationwide due to reports of 15mm connector disconnection from the tube during use.

    Product
    Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780055
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1829-2023·2023-07-05

    Slick Set Endotracheal Tubes recalled for connector disconnection risk

    Teleflex is recalling Slick Set Cuffed Endotracheal Tubes nationwide due to reported disconnection of the 15mm connector from the tube, affecting airway management in critical care settings.

    Product
    Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170060
    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-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-1902-2023·2023-07-05

    Slick Set Endotracheal Tubes Recalled for Connector Disconnection

    Teleflex is recalling 870 units of Slick Set Uncuffed Endotracheal Tubes nationwide due to reports of disconnection of the 15mm connector from the tube.

    Product
    Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150030
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1853-2023·2023-07-05

    Flexi-Set Cuffed Endotracheal Tube and Stylet Connector Disconnection Recall

    TELEFLEX LLC is recalling 13,710 units of Flexi-Set Cuffed Endotracheal Tubes due to reports of connector disconnection. The 15mm connector may separate from the tube during use.

    Product
    Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504590
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1868-2023·2023-07-05

    TELEFLEX Preformed Endotracheal Tube Recall for Connector Disconnection Risk

    TELEFLEX is recalling 1,570 units of Preformed AGT Oral Endotracheal Tubes nationwide due to reports of 15mm connector disconnection from the tubes. The disconnection could compromise airway management during patient ventilation.

    Product
    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180065
    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
  • SevereNHTSA·23V255000·2023-07-04

    Volvo VNR Trucks Recalled for Aggressive Adaptive Cruise Control Braking

    Volvo Trucks is recalling 2020-2023 VNR Electric vehicles equipped with Adaptive Cruise Control that can trigger aggressive braking under light load conditions, risking rear axle skidding and loss of vehicle control.

    Product
    VOLVO — 2021 VOLVO VNR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23234·2023-06-29

    Bose Acoustimass, Lifestyle, and Companion Bass Modules Due to Fire Hazard

    Bose Corporation is recalling select bass modules manufactured before April 2006 because electrical components can fail and cause fires. The firm has received 21 reports of ignition or melting worldwide, with three resulting in property damage.

    Product
    Bose Acoustimass, Lifestyle and Companion bass modules (produced before April 2006)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1798-2023·2023-06-28

    Implantable Cardioverter Defibrillators May Fail To Deliver Therapy; Class I Recall

    Medtronic implantable cardioverter defibrillators (ICDs) may fail to deliver high-voltage therapy due to a manufacturing defect in a specific feedthrough component. 447 units are affected worldwide.

    Product
    ICD-VR DVBB2D4 EVERA XT DF4 INTL, Model Number DVBB2D4; Implantable Cardioverter Defibrillators
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1803-2023·2023-06-28

    Implantable Cardioverter Defibrillators Recalled for Potential High Voltage Therapy Failure

    Medtronic implantable cardioverter defibrillators (ICDs) with a specific feedthrough component may have reduced or absent energy output during high voltage therapy. The FDA Class I recall affects 12,099 units distributed nationwide and worldwide.

    Product
    ICD-VR DVFB1D1 VISIA AF MRI US DF1, Model Number DVFB1D1; Implantable Cardioverter Defibrillators
    Category
    Medical Device
    Distribution
    Distributed nationwide