ANCHORFAST
Received Jul 2, 2026 · Event occurred Jun 29, 2026
Report 1119193-2026-00047 · MDR key 25693792
Device
Generic name
Oral Endotracheal Tube Fastener
Manufacturer
Hollister IncorporatedCatalog number
9799
Lot number
5F242
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
NA · Unknown
- Unspecified Tissue Injury
Narrative
Description of Event or Problem
THIS IS THE 1ST OF TWO REPORTS FROM THE SAME ACCOUNT. IT WAS REPORTED THAT A PATIENT EXPERIENCED CHEEK AND UPPER LIP PRESSURE AND SKIN BREAKDOWN WHILE USING THE HOLLISTER ANCHORFAST ENDOTRACHEAL TUBE HOLDER. ADDITIONALLY, IT WAS REPORTED THAT THE PATIENT NEEDED DEBRIDEMENT AND SUTURE REPAIR OF THE DEFECT. NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME.
Additional Manufacturer Narrative
DHR REVIEW COMPLETED AND WAS FOUND TO BE COMPLETE AND ACCURATE. THE DEVICE WAS NOT AVAILABLE FOR RETURN, SO DEVICE EXAMINATION WAS NOT POSSIBLE. THE ROOT CAUSE FOR THE REPORTED ISSUE IS NOT KNOWN.