Device recall
Z-1115-2013: Product is distributed by Zimmer (Warsaw, Indiana)/Synvasive Technology, Inc…
FDA device recall · Class II · Synvasive Technology Inc
Key facts
| Recall number (Z-number) | Z-1115-2013 |
|---|---|
| Recall event | 64810 |
| Product | Product is distributed by Zimmer (Warsaw, Indiana)/Synvasive Technology, Inc. (El Dorado Hills, CA) & manufactured under Synvasive Technology, Inc. El Dorado Hills, CA Reciprocating saw blade: A sterile surgical saw blade used to resect damaged cartilage and/or bond in an orthopaedic reconstructive… |
| Product code | GFA |
| Recalling firm | Synvasive Technology Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 15, 2014 |
| FEI number | 1000123893 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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