Device recall
Z-1994-2021: 5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with 70 cm Guidewire Unit…
FDA device recall · Class II · Bard Access Systems Inc.
Key facts
| Recall number (Z-number) | Z-1994-2021 |
|---|---|
| Recall event | 88057 |
| Product | 5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with 70 cm Guidewire Unit Label: PowerPICC REF CK000340B BARD MYPICC KIT 5F French Size Dual-Lumen 70cm Guidewire |
| Product code | LJS |
| Recalling firm | Bard Access Systems Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 31, 2023 |
| FEI number | 3006260740 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database