Reported May 24, 2023 · Ongoing
HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004
Access Vascular, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Access Vascular, Inc · 749 Middlesex Tpke · Billerica, MA · 01821-3906
Is this the product you have?
HydroPICC 4Fr Single Lumen CatheterMaximal Barrier KitModel Number 80001004
- Lot codes and dates
- UDI-DI00862559000487
- Lot Number11423949
- Amount recalled
- 240 units
Where it was sold
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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