Anspach Carbide Cutting Burrs & Drums: 1 — Class II medical device recall Z-0728-2014
Terminated recall by The Anspach Effort, Inc., reported 2014-01-22, distributed nationwide. Some carbide cutting burr fractured during use.
| Recall number | Z-0728-2014 |
|---|---|
| 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 | 2013-12-17 |
| Classified | 2014-01-13 |
| Reported by FDA | 2014-01-22 |
| Terminated | 2016-05-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, CH, IL, PL, ZA |
| Quantity | 28,562 of |
| Reason classes | device malfunction |
| Model numbers | S-15DRMC |
Product
Anspach Carbide Cutting Burrs & Drums: 1.5MM x 7.5MM Cylindrical Carbide Drum part # S-15DRMC Anspach cutting burrs are intended for cutting and shaping bone, including the spine and cranium
Reason for recall
Some carbide cutting burr fractured during use.
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-0728-2014. 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.