Device recall
Z-0800-03: Z2 Guiding Catheter 6 F JR3.5 SH Item No.: Z26JR35SH
FDA device recall · Class III · Medtronic, Inc.
Key facts
| Recall number (Z-number) | Z-0800-03 |
|---|---|
| Recall event | 25847 |
| Product | Z2 Guiding Catheter 6 F JR3.5 SH Item No. : Z26JR35SH |
| Recalling firm | Medtronic, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Feb 19, 2008 |
| 510(k) numbers | K981198 |
| FEI number | 1220452 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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