Device recall
Z-2127-2009: Stryker Orthopaedics Cancellous Bone Screw; Dia 5.5 mm; Lnth: 25 mm; Sterile…
FDA device recall · Class III · Stryker Howmedica Osteonics Corp.
Key facts
| Recall number (Z-number) | Z-2127-2009 |
|---|---|
| Recall event | 52713 |
| Product | Stryker Orthopaedics Cancellous Bone Screw; Dia 5.5 mm; Lnth: 25 mm; Sterile: Made in the USA; Stryker Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The bone screws are optional fixtures that may be used during knee and hip replacement procedures. |
| Product code | HWC |
| Recalling firm | Stryker Howmedica Osteonics Corp. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 27, 2010 |
| 510(k) numbers | K873251 |
| FEI number | 3003070421 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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