Device recall
Z-1672-2010: Mallory Head Calcar Femoral, 34 mm resection/porous coated, 15.0 mm x 220 mm…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-1672-2010 |
|---|---|
| Recall event | 55365 |
| Product | Mallory Head Calcar Femoral, 34 mm resection/porous coated, 15.0 mm x 220 mm right stem, Sterile, REF 11-104953, Biomet Orthopaedics, Warsaw, IN. Implant device intended for use in femoral revision surgery. |
| Product code | LPH |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 18, 2010 |
| 510(k) numbers | K031693 |
| FEI number | 1825034 |
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