ANSPACH Cutting bur — Class II medical device recall Z-1574-2014
Terminated recall by The Anspach Effort, Inc., reported 2014-05-21, distributed nationwide. Anspach product code L-3SD contained product code S-3SD which is shorter in length than the labeled product.
| Recall number | Z-1574-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Anspach Effort, Inc., Palm Beach Gardens, FL, United States |
| Recall initiated | 2014-01-08 |
| Classified | 2014-05-09 |
| Reported by FDA | 2014-05-21 |
| Terminated | 2015-01-20 |
| Distributed | Nationwide (US) |
| Quantity | 30 cutting |
| Reason classes | labeling |
| Serial numbers | G323081803 |
| Model numbers | L-3SD |
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 for recall
Anspach product code L-3SD contained product code S-3SD which is shorter in length than the labeled product.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1574-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.