Device recall
Z-0486-2010: E-Z CLEAN Non Stick Cautery Tip. Label reads in part: "MEGADYNE 11506 SOUTH…
FDA device recall · Class III · Megadyne Medical Products, Inc.
Key facts
| Recall number (Z-number) | Z-0486-2010 |
|---|---|
| Recall event | 53555 |
| Product | E-Z CLEAN Non Stick Cautery Tip. Label reads in part: "MEGADYNE 11506 SOUTH STATE STREET DRAPER, UTAH 84020 USA***CAT/REF 0029M E-Z CLEAN NON STICK CAUTERY TIP***STERILE *** Expiration Date: 2104-07***" The device is intended to conduct monopolar electrosurgical energy from an electrosurgical… |
| Product code | GEI |
| Recalling firm | Megadyne Medical Products, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Feb 17, 2010 |
| 510(k) numbers | K081791 |
| FEI number | 1721194 |
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