Drug recall
HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004
FDA recall event 92124 · Class II · Access Vascular, Inc
Key facts
| Event ID | 92124 |
|---|---|
| Recall numbers | Z-1605-2023 |
| Recalling firm | Access Vascular, Inc |
| Product type | Devices |
| Products | HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Mar 3, 2023 |
| Report date | May 24, 2023 |
| City | Billerica |
| State | MA |
| Country | United States |
| FEI number | 3021570645 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: