AnchorFast SlimFit recall
AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,
Why was AnchorFast SlimFit recalled?
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI/DI 00610075095834, Lot Numbers: 4L172, 4L182
- Product
- AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,
- Recalling firm
- Hollister Incorporated
- Quantity
- 45 box / 540 eaches
- Distribution
- Worldwide distribution - US Nationwide and the country of Canada.
- Recall date
- February 26, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)