Device recall
Z-0642-2007: Boston Scientific Medi-Tech(R) Katzen (TM) Infusion Wire, for the infusion of…
FDA device recall · Class III · Boston Scientific
Key facts
| Recall number (Z-number) | Z-0642-2007 |
|---|---|
| Recall event | 36979 |
| Product | Boston Scientific Medi-Tech(R) Katzen (TM) Infusion Wire, for the infusion of therapeutic agents (i.e. heparin, saline, thrombolytic agents, etc.) in the peripheral vasculature. The wire allows for the delivery of agents in either a 'pulse-spray' or 'slow weep' technique. Order No. REF: 46-193… |
| Product code | DQX |
| Recalling firm | Boston Scientific |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 20, 2007 |
| 510(k) numbers | K883880 |
| FEI number | 3002095335 |
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