RUSCH IPN044688Recalls & reported problems
Teleflex Incorporated · FLEXI-SET CUFFED STERILE · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 2
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
2 FDA recall records name this device's identifier, 2 still open.
34 other recalls cover devices cleared under the same FDA submission (K961837); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- May 25, 2023Open, Classified
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Z-1852-2023 · Root cause: Under Investigation by firm · FDA record ↗
- Dec 8, 2022Open, Classified
Potential for pilot balloon non-inflation or cuff non-deflation.
Z-1011-2023 · Root cause: Process control · FDA record ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K961837. One submission often covers many models, so check the product and lot details in each record.
- Z-1890-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082080
- Z-1892-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082090
- Z-1850-2023 · May 25, 2023 · Open, ClassifiedFlexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504575
- Z-1882-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080095
- Z-1883-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080100
- Z-1881-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080055
- Z-1888-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082070
- Z-1893-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082095
- Z-1958-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080050
- Z-1851-2023 · May 25, 2023 · Open, ClassifiedFlexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504580
- Z-1959-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080060
- Z-1849-2023 · May 25, 2023 · Open, ClassifiedFlexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504570
- Z-1964-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080085
- Z-1961-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080070
- Z-1899-2023 · May 25, 2023 · Open, ClassifiedRUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480045
…and 19 more.
Other Tube, tracheal (w/wo connector) devices
- Shiley 18875Covidien LP · Tube, tracheal (w/wo connector)4 deaths570 reports
- RUSCH IPN041476Teleflex Incorporated · Tube, tracheal (w/wo connector)10 recalls0 reports
- Shiley 18775Covidien LP · Tube, tracheal (w/wo connector)489 reports
- Shiley 18770Covidien LP · Tube, tracheal (w/wo connector)2 deaths434 reports
- Shiley 18880Covidien LP · Tube, tracheal (w/wo connector)2 deaths370 reports
- Shiley 18780Covidien LP · Tube, tracheal (w/wo connector)3 deaths286 reports
- Shiley 18770SCovidien LP · Tube, tracheal (w/wo connector)273 reports
- Shiley 18780SCovidien LP · Tube, tracheal (w/wo connector)251 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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