RUSCH IPN914318Recalls & reported problems
Teleflex Incorporated · Class 2
All models of RUSCH (220)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 14026704644893), received between Oct 29, 2021 and Oct 29, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Markings/Labelling Problem” (1 report).
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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- May 25, 2023Class IOpen, Classified
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Z-1839-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported problems
Device problems
- Device Markings/Labelling Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 29, 2021Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED "LETTERS AND MARKETING ARE COMING OFF WITH TAPE". UNKNOWN WHEN ISSUE WAS FIRST IDENTIFIED. UNKNOWN PATIENT CONDITION AT TIME OF REPORT. MULTIPLE ATTEMPTS FOR ADDITIONAL INFORMATION TO THE CUSTOMER HAVE BEEN UNSUCCESSFUL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12722062 ↗
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-1843-2023 · May 25, 2023 · Open, ClassifiedSlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170150
- Z-1835-2023 · May 25, 2023 · Open, ClassifiedSlick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170090
- Z-1833-2023 · May 25, 2023 · Open, ClassifiedSlick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170080
- Z-1897-2023 · May 25, 2023 · Open, ClassifiedRUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480035
- Z-1838-2023 · May 25, 2023 · Open, ClassifiedSlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170125
- Z-1841-2023 · May 25, 2023 · Open, ClassifiedSlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170140
- Z-1840-2023 · May 25, 2023 · Open, ClassifiedSlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170135
- Z-1903-2023 · May 25, 2023 · Open, ClassifiedSlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150035
- Z-1827-2023 · May 25, 2023 · Open, ClassifiedSlick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050
- Z-1905-2023 · May 25, 2023 · Open, ClassifiedSlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150055
- Z-1832-2023 · May 25, 2023 · Open, ClassifiedSlick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170075
- Z-1836-2023 · May 25, 2023 · Open, ClassifiedSlick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170095
- Z-1844-2023 · May 25, 2023 · Open, ClassifiedSlick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170155
- Z-1860-2023 · May 25, 2023 · Open, ClassifiedSlick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 1700100
- 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 and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page