Device recall
Z-2580-2011: MTD 4000 - Mettler Traction Decompression System, Model: ME 4000 Product Usage…
FDA device recall · Class II · Mettler Electronics Corp
Key facts
| Recall number (Z-number) | Z-2580-2011 |
|---|---|
| Recall event | 58787 |
| Product | MTD 4000 - Mettler Traction Decompression System, Model: ME 4000 Product Usage: Provide traction and mobilization of skeletal structures and skeletal muscles |
| Product code | ITH |
| Recalling firm | Mettler Electronics Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 10, 2012 |
| 510(k) numbers | K091540 |
| FEI number | 2013558 |
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