Device recall
Z-1676-2020: ZIMMER Oscillating Saw Blade -Cutting 75mm x 19mm x 1.00/1.27mm.intended for…
FDA device recall · Class II · Synvasive Technology Inc
Key facts
| Recall number (Z-number) | Z-1676-2020 |
|---|---|
| Recall event | 85223 |
| Product | ZIMMER Oscillating Saw Blade -Cutting 75mm x 19mm x 1.00/1.27mm.intended for bone or cartilage in orthopedic procedures. Manufactured By: Synvasive Technology, Inc., a Subsidiary of Zimmer |
| Product code | GFA |
| Recalling firm | Synvasive Technology Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 7, 2021 |
| 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