Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short Recalled by Access Vascular, Inc Due to Mislabeling
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Access Vascular, Inc directly.
Affected Products
HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short term access (<30days) to the peripheral venous access system for intravenous therapy Product Model Number: 80004004
Quantity: 155 units
Why Was This Recalled?
Product Mislabeled on the outer bag and inner kit Tyvek header bag
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Access Vascular, Inc
Access Vascular, Inc has 8 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report