FDA Medical Device Recalls (openFDA)
Hollister Incorporated: AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787
- Recall number
- Z-1179-2025
- Recalling firm
- Hollister Incorporated
- Product
- AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,
- Status
- Open, Classified
- Initiated
- 2024-12-23
- Posted
- 2025-02-19
- Terminated
- not on file
- Reason
- Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
- Root cause
- Process change control
- Action
- Hollister issued an URGENT - MEDICAL DEVICE RECALL notice to its consignees on 12/23/2024 via FedEx and email. The notice explained the reason for the recall and potential risk and instructed customers to quarantine affected inventory, discard the product per their local procedures for product destruction, and Please complete and return the response form attached as soon as possible, even if you do not have affected product in your possession and send to ComplaintCommunication@Hollister.com. For product credit requests: If you are a direct customer of Hollister, contact Hollister Incorporated Customer Service for product credit at: 1-800-323-4060 (prompt #1). If you purchase product from a distributor, please contact your distributor for product credit. Hollister has posted this recall on their website with the link to the page.
- Quantity
- 45 box / 540 eaches
- Distribution
- Worldwide distribution - US Nationwide and the country of Canada.
- Lot, serial or model codes
- UDI/DI 00610075095834, Lot Numbers: 4L172, 4L182
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- CBH
- Firm FEI
- 1480288
- Firm city
- Libertyville
- Firm state
- IL
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28