FDA Device recall Z-1574-2014
ANSPACH Cutting bur, 3 mm Diamond Ball, Standard Length
- FDA Device
- Class II
- terminated
- Published 2014-05-21
On 2014-05-21 the FDA classified a Class II recall of ANSPACH Cutting bur, 3 mm Diamond Ball, Standard Length by The Anspach Effort, citing anspach product code L-3SD contained product code S-3SD which is shorter in length than the labeled product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1574-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-01-08 |
| Published | 2014-05-21 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | The Anspach Effort |
| Distribution | US |
Product
ANSPACH Cutting bur, 3 mm Diamond Ball, Standard Length. REF L-3SD Use with LONG Attachments. Used for cutting and shaping bone, including the spine and cranium.
Reason
Anspach product code L-3SD contained product code S-3SD which is shorter in length than the labeled product.
Identifiers
| code_info | Lot/Set/Serial: G323081803. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1574-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.