FDA recall Z-1179-2025

Hollister Incorporated · Class II · device

Product

AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,

Reason for recall

Hollister received reports of decreased skin barrier wear time which could can lead to tube migration

Distribution

Worldwide distribution - US Nationwide and the country of Canada.

Key facts

Status
Ongoing
Initiation date
2024-12-23
Report date
2025-02-26
Voluntary/Mandated
Voluntary: Firm initiated
Location
Libertyville, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1179-2025