Device recall
Z-0666-03: Medi-Tech Magic Torque Glidex hydrophilic coated guidewire,.035 inch/180 cm and…
FDA device recall · Class III · Symbiosis Corp.
Key facts
| Recall number (Z-number) | Z-0666-03 |
|---|---|
| Recall event | 25704 |
| Product | Medi-Tech Magic Torque Glidex hydrophilic coated guidewire, .035 inch/180 cm and .035 inch/260 cm lengths. Packaged in a sterile pouch and a three pack shelf box. |
| Product code | DQX |
| Recalling firm | Symbiosis Corp. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 13, 2012 |
| 510(k) numbers | K933334 |
| FEI number | 1051710 |
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