Device recall
Z-1343-2015: TUBING 7/8' X 10', W/WAND & TIP, 24/CS, REF 24187, QTY 24\CS, STERILE EO…
FDA device recall · Class II · Microtek Medical Inc
Key facts
| Recall number (Z-number) | Z-1343-2015 |
|---|---|
| Recall event | 70721 |
| Product | TUBING 7/8' X 10', W/WAND & TIP, 24/CS, REF 24187, QTY 24\CS, STERILE EO Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures. Locations include Operating Rooms, Trauma, Endoscopy and… |
| Product code | FYD |
| Recalling firm | Microtek Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 21, 2017 |
| 510(k) numbers | K001082 |
| FEI number | 1043582 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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