Device recall
Z-2709-2011: Product Brand Name: Versafitcup Double Mobility Liner Inserter Product Generic…
FDA device recall · Class II · Medacta Usa Inc
Key facts
| Recall number (Z-number) | Z-2709-2011 |
|---|---|
| Recall event | 59043 |
| Product | Product Brand Name: Versafitcup Double Mobility Liner Inserter Product Generic Name: Versafitcup Double Mobility Liner Inserter Model Number: 01.26.10.0018 The hip prosthesis is designed for cementless use in total hip arthroplasty in primary or revision surgery. The patient should be skeletally… |
| Product code | MEH |
| Recalling firm | Medacta Usa Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 12, 2011 |
| 510(k) numbers | K083116 |
| 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