AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,
Reported: February 26, 2025 Initiated: December 23, 2024 #Z-1179-2025
Product Description
AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,
Reason for Recall
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Details
- Recalling Firm
- Hollister Incorporated
- Units Affected
- 45 box / 540 eaches
- Distribution
- Worldwide distribution - US Nationwide and the country of Canada.
- Location
- Libertyville, IL
Frequently Asked Questions
What product was recalled? ▼
AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,. Recalled by Hollister Incorporated. Units affected: 45 box / 540 eaches.
Why was this product recalled? ▼
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 26, 2025. Severity: Moderate. Recall number: Z-1179-2025.
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