Device recall: AnchorFast Guard Select, Oral Endotracheal Tube Fastener, REF 9700,
Class II FDA enforcement event 96181. Recall start date: . Status in the FDA record: Ongoing.
Reason for recall, in the words of FDA
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Hollister Incorporated started this device recall on 23 Dec 2024. The firm address in the FDA record is in Libertyville, IL. FDA put the recall in Class II. FDA event 96181 has 4 product records. The first FDA enforcement report date is 26 Feb 2025. The record gives the status Ongoing.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
Worldwide distribution - US Nationwide and the country of Canada.
Recalling firm
Hollister Incorporated, Libertyville, IL.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
4 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-1178-2025 | AnchorFast Guard Select, Oral Endotracheal Tube Fastener, REF 9700, | 701 box / 8,412 eaches | Class II | Ongoing | 26 Feb 2025 |
| Z-1179-2025 | AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787, | 45 box / 540 eaches | Class II | Ongoing | 26 Feb 2025 |
| Z-1180-2025 | AnchorFast, Oral Endotracheal Tube Fastener, REF 9799, | 30,527 box / 366,324 eaches | Class II | Ongoing | 26 Feb 2025 |
| Z-1181-2025 | AnchorFast Guard, Oral Endotracheal Tube Fastener, REF 9800, | 4,955 box / 59,460 eaches | Class II | Ongoing | 26 Feb 2025 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Device events that started in 2024
- 970
- Share of these events in Class II
- 87%
- Product records in this event
- 4Median of the firm: 4
- Events of the firm on the register
- 2
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 11 Feb 2021 | Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and accessories) - Product Usage: designed to stabil Event 87351 | Device | Class II | 1 |
Official channels
- FDA enforcement report Z-1178-2025The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
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Cite this page
Recall Register. FDA enforcement event 96181. https://recallregister.com/fda/ii/96181/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA device enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
Worldwide distribution - US Nationwide and the country of Canada.
- What quantity of product is in FDA event 96181?
- The event has 4 product records. The first record gives this quantity:
701 box / 8,412 eaches
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many device recalls of 2024 have the same class?
- 87% of the 970 device events that started in 2024 are in Class II.