AnchorFast — Class II medical device recall Z-1180-2025
Ongoing recall by Hollister Incorporated, reported 2025-02-26, distributed nationwide. Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
| Recall number | Z-1180-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hollister Incorporated, Libertyville, IL, United States |
| Recall initiated | 2024-12-23 |
| Classified | 2025-02-19 |
| Reported by FDA | 2025-02-26 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| UPC / GTIN / UDI-DI | 00610075129386 |
| Lot numbers | 4I192, 4I202, 4I212, 4I222, 4I232, 4I242, 4I252, 4I262, 4I272, 4I282, 4I292, 4I302, 4J012, 4J022, 4J032, 4J042, 4J052, 4J062, 4J072, 4J082, 4J092, 4J102, 4J112, 4J122, 4J132, 4J142, 4J152, 4J162, 4J212, 4J222, 4J232, 4J242, 4J252, 4J262, 4J272, 4J282, 4J292, 4J302, 4J312, 4K012 and 42 more |
| Model numbers | 9799 |
Product
AnchorFast, Oral Endotracheal Tube Fastener, REF 9799,
Reason for recall
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1180-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.