Device recall
Z-1906-2023: Icelock 125 Ratchet, REF: L-125000; Icelock 600XM Ratchet, REF: L-621200…
FDA device recall · Class II · Ossur H / F
Key facts
| Recall number (Z-number) | Z-1906-2023 |
|---|---|
| Recall event | 92207 |
| Product | Icelock 125 Ratchet, REF: L-125000; Icelock 600XM Ratchet, REF: L-621200; Icelock 621 Ratchet, REF: L-621000; Icelock 621 Ratchet Adaption Kit, REF: L-621100; Ratchet Lock Body, REF: L-692020 |
| Product code | ISH |
| Recalling firm | Ossur H / F |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3003764610 |
At a glance
- None Linked 510(k)s
- 1–9 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