Device recall
Z-1382-2009: Short Citation TMZF HA Hip Stem - Right; Hydroxylapatite Coated, Titanium Plasma…
FDA device recall · Class II · Stryker Howmedica Osteonics Corp.
Key facts
| Recall number (Z-number) | Z-1382-2009 |
|---|---|
| Recall event | 50901 |
| Product | Short Citation TMZF HA Hip Stem - Right; Hydroxylapatite Coated, Titanium Plasma Spray; V40 Taper, 132 degree neck angle: Stem Length - 102mm; Head Offset - 52mm, Distal Diameter - 16mm. Hip stems are single use devices intended for cementless fixation. The products are intended for use in primary… |
| Product code | MEH |
| Recalling firm | Stryker Howmedica Osteonics Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 25, 2012 |
| 510(k) numbers | K993768 |
| 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