Device recall
Z-2120-2017: StatLock IV Premium Catheter Stabilization Device, product code IV0570. sterile…
FDA device recall · Class II · Bard Access Systems Inc.
Key facts
| Recall number (Z-number) | Z-2120-2017 |
|---|---|
| Recall event | 77132 |
| Product | StatLock IV Premium Catheter Stabilization Device, product code IV0570. sterile. Packaging: packaged as single units in tyvek to film pouches, the product is distributed in cartons containing 25 devices and cases containing 250 devices. |
| Product code | KMK |
| Recalling firm | Bard Access Systems Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 21, 2017 |
| FEI number | 3006260740 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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