Device recall
Z-0702-2017: MANOS EX (CAT#TY-12-101) Product Usage: Carpal Tunnel Release: as a tool for…
FDA device recall · Class II · Thayer Intellectual Property, Inc.
Key facts
| Recall number (Z-number) | Z-0702-2017 |
|---|---|
| Recall event | 75630 |
| Product | MANOS EX (CAT#TY-12-101) Product Usage: Carpal Tunnel Release: as a tool for tissue release of the transverse carpal ligament in patients with Carpal Tunnel Syndrome who fail conservative therapy. Plantar Fasciotomy: as a tool for tissue recession in patients with plantar fasciitis who fail… |
| Product code | LXH |
| Recalling firm | Thayer Intellectual Property, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 13, 2017 |
| FEI number | 3008792617 |
At a glance
- None 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