RUSCH IPN042495Recalls & reported problems
Teleflex Incorporated · SLICK SET UNCUFFED STERILE · Class 2
1 open recall names 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
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
27 other recalls cover devices cleared under the same FDA submission (K780900); 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-1901-2023 · Root cause: Under Investigation by firm · FDA record ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K780900. One submission often covers many models, so check the product and lot details in each record.
- Z-1830-2023 · May 25, 2023 · Open, ClassifiedSlick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170065
- Z-1840-2023 · May 25, 2023 · Open, ClassifiedSlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170135
- Z-1900-2023 · May 25, 2023 · Open, ClassifiedSlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150020
- Z-1902-2023 · May 25, 2023 · Open, ClassifiedSlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150030
- Z-1827-2023 · May 25, 2023 · Open, ClassifiedSlick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050
- Z-1843-2023 · May 25, 2023 · Open, ClassifiedSlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170150
- Z-1860-2023 · May 25, 2023 · Open, ClassifiedSlick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 1700100
- Z-1835-2023 · May 25, 2023 · Open, ClassifiedSlick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170090
- Z-1829-2023 · May 25, 2023 · Open, ClassifiedSlick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170060
- Z-1833-2023 · May 25, 2023 · Open, ClassifiedSlick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170080
- Z-1834-2023 · May 25, 2023 · Open, ClassifiedSlick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170085
- Z-1839-2023 · May 25, 2023 · Open, ClassifiedSlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170130
- Z-1832-2023 · May 25, 2023 · Open, ClassifiedSlick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170075
- Z-1842-2023 · May 25, 2023 · Open, ClassifiedSlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170145
- Z-1837-2023 · May 25, 2023 · Open, ClassifiedSlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170120
…and 12 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.