Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
HydroPICC 4Fr Single Lumen Catheter Recalled by Access Vascular, Inc Due to The catheter packaged with specific lots of the...
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
HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004
Quantity: 240 units
Why Was This Recalled?
The catheter packaged with specific lots of the HydroPICC Kits and HydroMID Kits have a shorter expiration date than what is listed on the outer kit package.
Where Was This Sold?
This product was distributed to 3 states: FL, TN, TX
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