Device recall
Z-2212-2010: DYNASTY A-CLASS POLY LINER, REF DLXP-LD36, 1 EACH, Rx ONLY, STERILE EO, GROUP D…
FDA device recall · Class III · Wright Medical Technology Inc
Key facts
| Recall number (Z-number) | Z-2212-2010 |
|---|---|
| Recall event | 56131 |
| Product | DYNASTY A-CLASS POLY LINER, REF DLXP-LD36, 1 EACH, Rx ONLY, STERILE EO, GROUP D, I.D. 36 mm, LIP 15o, LINER STD, Wright Medical Technology, 4677 Airline Road, Arlington, TN 38002. Product is used in total hip arthroplasty. |
| Product code | JDL |
| Recalling firm | Wright Medical Technology Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 31, 2011 |
| 510(k) numbers | K082924 |
| FEI number | 1043534 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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