RUSCH IPN041476Recalls & reported problems
Teleflex Incorporated · ENDOTRACHEAL TUBE - WITH CUFF - MAGILL - STERILE PACK · Class 2
10 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
- 10
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
10 FDA recall records name this device's identifier, 10 still open.
26 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-1882-2023 · Root cause: Under Investigation by firm · FDA record ↗
- May 25, 2023Open, Classified
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Z-1963-2023 · Root cause: Under Investigation by firm · FDA record ↗
- May 25, 2023Open, Classified
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Z-1960-2023 · Root cause: Under Investigation by firm · FDA record ↗
- May 25, 2023Open, Classified
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Z-1964-2023 · Root cause: Under Investigation by firm · FDA record ↗
- May 25, 2023Open, Classified
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Z-1883-2023 · Root cause: Under Investigation by firm · FDA record ↗
- May 25, 2023Open, Classified
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Z-1881-2023 · Root cause: Under Investigation by firm · FDA record ↗
- May 25, 2023Open, Classified
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Z-1965-2023 · Root cause: Under Investigation by firm · FDA record ↗
- May 25, 2023Open, Classified
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Z-1959-2023 · Root cause: Under Investigation by firm · FDA record ↗
- May 25, 2023Open, Classified
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Z-1961-2023 · Root cause: Under Investigation by firm · FDA record ↗
- May 25, 2023Open, Classified
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Z-1958-2023 · Root cause: Under Investigation by firm · 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-1849-2023 · May 25, 2023 · Open, ClassifiedFlexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504570
- Z-1847-2023 · May 25, 2023 · Open, ClassifiedFlexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504560
- Z-1893-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082095
- Z-1850-2023 · May 25, 2023 · Open, ClassifiedFlexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504575
- Z-1962-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080075
- Z-1892-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082090
- Z-1845-2023 · May 25, 2023 · Open, ClassifiedFlexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504550
- Z-1848-2023 · May 25, 2023 · Open, ClassifiedFlexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504565
- Z-1851-2023 · May 25, 2023 · Open, ClassifiedFlexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504580
- Z-1890-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082080
- Z-1887-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082065
- Z-1889-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082075
- Z-1884-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082050
- Z-1886-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082060
- Z-1885-2023 · May 25, 2023 · Open, ClassifiedEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082055
…and 11 more.
Other Tube, tracheal (w/wo connector) devices
- Shiley 18875Covidien LP · Tube, tracheal (w/wo connector)4 deaths570 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
- Portex 100/199/075Icu Medical, Inc. · Tube, tracheal (w/wo connector)4 deaths222 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.