Data Foundry

Medical device recalls 2014

Anspach Carbide Cutting Burrs: 1 — Class II medical device recall Z-0727-2014

Terminated recall by The Anspach Effort, Inc., reported 2014-01-22, distributed nationwide. Some carbide cutting burr fractured during use.

Recall numberZ-0727-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmThe Anspach Effort, Inc., Palm Beach Gardens, FL, United States
Recall initiated2013-12-17
Classified2014-01-13
Reported by FDA2014-01-22
Terminated2016-05-09
DistributedNationwide (US)
Countries outside the USAU, CA, CH, IL, PL, ZA
Quantity28,562 of
Reason classesdevice malfunction
Model numbers1MM, 2MM, 3MM, 4MM, 5MM, 6MM, S-15DRMC-L, S-1B-C, S-2SB-C, S-3B-C, S-3SB-C, S-4B-C, S-4BL-C, S-5B-C, S-6B-C

Product

Anspach Carbide Cutting Burrs: 1.5MMx7.5MM Cylindrical Carbide Drum part # S-15DRMC-L, 1MM Carbide Fluted ball, Extended part # S-1B-C, 1MM Carbide Fluted ball part # S-SB-C, 2MM Carbide Fluted ball part # S-2SB-C, 3MM Carbide Fluted ball Extended part # S-3B-C, 3MM Carbide Fluted ball part # S-3SB-C, 4MM Carbide Fluted ball part # S-4B-C, 4MM Carbide Fluted ball Extended 27MM part # S-4BL-C, 5MM Carbide Fluted ball part # S-5B-C, and 6MM Carbide Fluted ball part # S-6B-C. 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-0727-2014. 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.