FDA Device recall Z-2839-2016
G1 Dissection Tool - 3mm FLUTED BALL
- 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 FLUTED BALL 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-2839-2016 |
| 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 FLUTED BALL; 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-3SB-2-G1 Batch J316017640 |
|---|
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-2839-2016%22
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