Device recall
Z-1699-2015: M/L Taper with Kinectiv Technology. prosthesis, hip, semi-constrained (metal…
FDA device recall · Class I · Zimmer, Inc.
Key facts
| Recall number (Z-number) | Z-1699-2015 |
|---|---|
| Recall event | 71272 |
| Product | M/L Taper with Kinectiv Technology. prosthesis, hip, semi-constrained (metal uncemented acetabular component) Product Usage: Usage: Total hip replacement for the following: severe hip pain and disability due to rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis, collagen… |
| Product code | KWA |
| Recalling firm | Zimmer, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 2, 2016 |
| 510(k) numbers | K071856 |
| FEI number | 1000220733 |
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