Device recall
Z-0196-2019: Medacta International MiniMAX CEMENTLESS ANATOMICAL STEM, 12/14: for cementless…
FDA device recall · Class II · Medacta Usa Inc
Key facts
| Recall number (Z-number) | Z-0196-2019 |
|---|---|
| Recall event | 81090 |
| Product | Medacta International MiniMAX CEMENTLESS ANATOMICAL STEM, 12/14: for cementless use in total or partial hip arthroplasty in primary or revision surgery. |
| Product code | LZO |
| Recalling firm | Medacta Usa Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 29, 2019 |
| 510(k) numbers | K170845 |
| FEI number | 3006639916 |
At a glance
- 1–9 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