Device recall
Z-2207-2010: Monarch Labs Medical Maggots with the accessory LeFlap dressing (previously…
FDA device recall · Class II · Monarch Labs, LLC
Key facts
| Recall number (Z-number) | Z-2207-2010 |
|---|---|
| Recall event | 56031 |
| Product | Monarch Labs Medical Maggots with the accessory LeFlap dressing (previously known as Creature Comforts II), 250-500 per vial, Batch #: MM-090406 with CCII-0901. Maggot therapy is intended to debride serious non-healing (chronic) wounds, and the dressing intended to confine the maggots to the wound. |
| Product code | NQK |
| Recalling firm | Monarch Labs, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 13, 2012 |
| 510(k) numbers | K072438 |
| FEI number | 3005735989 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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