Device recall
Z-0444-2009: Medtronic Input TS 7F 11 cm Ref: 071102A Percutaneous catheter introducer sets…
FDA device recall · Class II · Medtronic, Inc.
Key facts
| Recall number (Z-number) | Z-0444-2009 |
|---|---|
| Recall event | 50078 |
| Product | Medtronic Input TS 7F 11 cm Ref: 071102A Percutaneous catheter introducer sets, including sheath, dilator, guide wire and needle, are used to facilitate placing a catheter through the skin into a vein or artery. Percutaneous introducers are recommended for initial percutaneous introduction or the… |
| Product code | DYB |
| Recalling firm | Medtronic, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 7, 2011 |
| 510(k) numbers | K955785 |
| FEI number | 1220452 |
At a glance
- 1–9 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