Class II — Hollister Incorporated
| Recalling firm | Hollister Inc. |
|---|---|
| Registered facility | View this company's 7 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Hollister received reports of decreased skin barrier wear time which could can lead to tube migration |
| Product | AnchorFast Guard, Oral Endotracheal Tube Fastener, REF 9800, |
| Quantity | 4,955 box / 59,460 eaches |
| Distribution | Worldwide distribution - US Nationwide and the country of Canada. |
| Initiated | 2024-12-23 |
| Classified | 2025-02-19 |
| Recall number | Z-1181-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Hollister Incorporated (Z-1181-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/96181/
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