HydroPICC 4Fr Single Lumen Catheter — Class II medical device recall Z-1605-2023
Ongoing recall by Access Vascular, Inc, reported 2023-05-24, distributed in FL, TN, TX. The catheter packaged with specific lots of the HydroPICC Kits and HydroMID Kits have a shorter expiration dat
| Recall number | Z-1605-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Access Vascular, Inc, Billerica, MA, United States |
| Recall initiated | 2023-03-03 |
| Classified | 2023-05-18 |
| Reported by FDA | 2023-05-24 |
| Distributed | FL, TN, TX |
| Quantity | 240 units |
| UPC / GTIN / UDI-DI | 00862559000487 |
| Lot numbers | 11423949 |
| Model numbers | 80001004 |
Product
HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1605-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.