Drug recall
5Fr PowerPICC Catheter Single-Lumen with 70cm Guidewire Instructions For Use: PowerPicc Polyurethand Radiology…
FDA recall event 88048 · Class II · Bard Access Systems Inc.
Key facts
| Event ID | 88048 |
|---|---|
| Recall numbers | Z-1991-2021 |
| Recalling firm | Bard Access Systems Inc. |
| Product type | Devices |
| Products | 5Fr PowerPICC Catheter Single-Lumen with 70cm Guidewire Instructions For Use: PowerPicc Polyurethand Radiology PiCC with Microintroducer |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Catheter kits contained the incorrect micro-introducers. |
| Initiation date | May 19, 2021 |
| Report date | Jul 7, 2021 |
| Termination date | Jan 24, 2023 |
| City | Salt Lake City |
| State | UT |
| Country | United States |
| FEI number | 3006260740 |
At a glance
- 1–9 Products in this recall
- 10–99 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: