FDA Device recall Z-2838-2016
G1 Dissection Tool - 3mm CRS DBALL, 2mm SHAFT EXP, M
- FDA Device
- Class II
- terminated
- Published 2016-09-28
On 2016-09-28 the FDA classified a Class II recall of G1 Dissection Tool - 3mm CRS DBALL, 2mm SHAFT EXP, M by The Anspach Effort, citing the firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2838-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-08-26 |
| Published | 2016-09-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | The Anspach Effort |
| Distribution | AZ, CA, DC, MD, MI, OR |
Product
G1 Dissection Tool - 3mm CRS DBALL, 2mm SHAFT EXP, M; For cutting and shaping bone including spine and cranium.
Reason
The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.
Identifiers
| code_info | Material M-3DC-2-G1 Batch J313108568 & J316017637 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2838-2016%22
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