Device recall
Z-1229-2007: Guidewire, 70cm x 1mm, REF 5583705, Sterile, Single Use, BARD Access Systems…
FDA device recall · Class II · C.R. Bard Access Systems, Inc
Key facts
| Recall number (Z-number) | Z-1229-2007 |
|---|---|
| Recall event | 38621 |
| Product | Guidewire, 70cm x 1mm, REF 5583705, Sterile, Single Use, BARD Access Systems, Hemodialysis Catheter, Salt Lake City, UT 84116. |
| Product code | MPB |
| Recalling firm | C.R. Bard Access Systems, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 25, 2008 |
| 510(k) numbers | K844433 |
| FEI number | 3006260740 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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