Recall · FDA
The Anspach Effort, Inc.
The Anspach Effort, Inc. issued a Class II FDA recall (Z-2031-2017) initiated 2016-10-06: Sagittal MICRO-SAW
| Company | The Anspach Effort, Inc. |
|---|---|
| Recall number | Z-2031-2017 |
| Classification | Class II |
| Status | Terminated |
| Category | Devices |
| Initiated | 2016-10-06 |
| Product | Sagittal MICRO-SAW |
| Reason | Supplied Directions for Use (DFU) did not contain a recommended service interval. |
FAQ
What did The Anspach Effort, Inc. recall?
Sagittal MICRO-SAW
Why was The Anspach Effort, Inc.'s product recalled?
Supplied Directions for Use (DFU) did not contain a recommended service interval.