ANCHORFAST ORAL ENDOTRACHEAL TUBE FASTENER
Received Jun 23, 2026 · Event occurred May 22, 2026
Report 1119193-2026-00044 · MDR key 25599461
Device
Generic name
Anchorfast, Product Code: Cbh
Manufacturer
Hollister IncorporatedModel number
9799Lot number
UNKNOWN
Product problems
- Device Dislodged or Dislocated
Patient
16 YR · Male
- Unintended Extubation
Narrative
Additional Manufacturer Narrative
DHR REVIEW NOT POSSIBLE BECAUSE LOT NUMBER NOT PROVIDED. IT WAS NOT KNOWN IF THERE WAS ANY DEVICE ADHESION ISSUES OR IF THE ET TUBE SLIPPED THROUGH THE STRAP. THE ROOT CAUSE OF THE REPORTED EXTUBATIONS ARE NOT KNOWN. ONLY THE DI INFORMATION OF THE UDI IS KNOW DUE TO LACK OF LOT NUMBER.
Description of Event or Problem
IT WAS REPORTED THAT THE PATIENT'S ENDOTRACHEAL TUBE (ETT) BECAME DISLODGED DURING A COUGHING EPISODE. THE REGISTERED NURSE RESPONDED AND OBSERVED THAT THE ETT AND HOLLISTER'S ANCHORFAST ORAL ENDOTRACHEAL TUBE FASTENER HAD DETACHED FROM THE PATIENT. THE PATIENT REQUIRED REINTUBATION, NO OTHER DETAILS ARE AVAILABLE AT THIS TIME REGARDING THIS REPORTED EVENT.