FDA Device recall Z-1605-2023
HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004
- FDA Device
- Class II
- ongoing
- Published 2023-05-24
On 2023-05-24 the FDA classified a Class II recall of HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004 by Access Vascular, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1605-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-03-03 |
| Published | 2023-05-24 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Access Vascular |
| Distribution | FL, TN, TX |
Product
HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004
Reason
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.
Identifiers
| code_info | UDI-DI: 00862559000487; Lot Number: 11423949 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1605-2023%22
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