Device recall
Z-2199-2013: AEQUALIS Reversed II or AEQUALIS Reversed Fracture Impactor. These products are…
FDA device recall · Class II · Tornier, Inc
Key facts
| Recall number (Z-number) | Z-2199-2013 |
|---|---|
| Recall event | 66057 |
| Product | AEQUALIS Reversed II or AEQUALIS Reversed Fracture Impactor. These products are contained within the Aequalis reversed II Instrument set tray no.YKAD83 and the Aequalis reversed fracture instrument set tray no.YKAD95. The items affected are MWD21, MWD023, MWD024 and MWD025. The impactor is an… |
| Product code | HTZ |
| Recalling firm | Tornier, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 3, 2015 |
| FEI number | 3000718467 |
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