Hollister Incorporated: Device Recall
Recall #Z-1180-2025 · 12/23/2024
Class II: Risk
Recall Details
- Recall Number
- Z-1180-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Hollister Incorporated
- Status
- Ongoing
- Date Initiated
- 12/23/2024
- Location
- Libertyville, IL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 30,527 box / 366,324 eaches
Reason for Recall
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Product Description
AnchorFast, Oral Endotracheal Tube Fastener, REF 9799,
Distribution Pattern
Worldwide distribution - US Nationwide and the country of Canada.
Other Recalls by Hollister Incorporated
- Class II: Risk 12/23/2024
- Class II: Risk 12/23/2024
- Class II: Risk 12/23/2024
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.