Device recall
Z-0916-2007: AcuMatch M-Series Straight Fluted Stem Segment and AcuMatch M-Series Curved…
FDA device recall · Class II · Exactech, Inc.
Key facts
| Recall number (Z-number) | Z-0916-2007 |
|---|---|
| Recall event | 37788 |
| Product | AcuMatch M-Series Straight Fluted Stem Segment and AcuMatch M-Series Curved Fluted Stem Segment. Catalog numbers 150-07-19 and 150-07-44. |
| Product code | LPH |
| Recalling firm | Exactech, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 6, 2012 |
| 510(k) numbers | K993736 |
| FEI number | 1038671 |
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