AnchorFast Guard Select 9700Recalls & reported problems
Hollister Incorporated · Oral Endotracheal Tube Fastener · Class 1
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
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00610075095810), received between Dec 22, 2025 and Dec 22, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
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.
Reports received per month
Recalls naming this device
- Dec 23, 2024Open, Classified
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Z-1178-2025 · Root cause: Process change control · FDA record ↗
Most reported problems
Device problems
- Patient Device Interaction Problem1
Patient problems
- Tooth Loss1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 22, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
(B)(6) IN (B)(6) CANADA REPORTED AN INCIDENT INVOLVING ONE OF THEIR PATIENT'S THAT HAD A HOLLISTER SECUREMENT DEVICE ENDOTRACHEAL TUBE ANCHORFAST WITH BITEGUARD. IT WAS REPORTED THAT THE DEVICE WAS POSITIONED IN THE MIDDLE WHEN THE PATIENT BIT DOWN AND REPORTEDLY BROKE THREE OF THEIR BOTTOM INCISORS.
Patient problems: Tooth Loss
MAUDE report 23863024 ↗
Other DEVICE, FIXATION, TRACHEAL TUBE devices
- AnchorFast 9799Hollister Incorporated · DEVICE, FIXATION, TRACHEAL TUBE1 recall1 death49 reports
- AnchorFast SlimFit 9787Hollister Incorporated · DEVICE, FIXATION, TRACHEAL TUBE1 recall4 reports
- AnchorFast Guard 9800Hollister Incorporated · DEVICE, FIXATION, TRACHEAL TUBE1 recall4 reports
- Medline DYNJMBRC2Medline Industries, Inc. · DEVICE, FIXATION, TRACHEAL TUBE1 recall1 report
- Medline DYNJMBRC4BMedline Industries, Inc. · DEVICE, FIXATION, TRACHEAL TUBE1 recall0 reports
- AnchorFast 9799Hollister Incorporated · DEVICE, FIXATION, TRACHEAL TUBE21 reports
- HUDSON RCI IPN914324Teleflex Incorporated · DEVICE, FIXATION, TRACHEAL TUBE6 reports
- Dale Endotracheal Tube Holder 270Dale Medical Products, Inc. · Device, Fixation, Tracheal Tube6 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.