ANSPACH — Class II medical device recall Z-2298-2015
Terminated recall by The Anspach Effort, Inc., reported 2015-08-05, distributed in AZ, CA, CO, FL, GA, IL, KY, LA…. G1 Dissection Tools are not compatible with all attachments listed on the labeling; G1 cutting tools are label
| Recall number | Z-2298-2015 |
|---|---|
| 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 | 2015-04-13 |
| Classified | 2015-07-29 |
| Reported by FDA | 2015-08-05 |
| Terminated | 2016-08-25 |
| Distributed | AZ, CA, CO, FL, GA, IL, KY, LA, MN, MO, NC, NJ, NY, OH, OR, PA, TX |
| Countries outside the US | CA, CN |
| Quantity | 70 tools |
| Reason classes | labeling |
| Model numbers | M-6DC-2-G1 |
Product
ANSPACH - 6MM Coarse Diamond Ball, 2 mm Shaft Exposure; REF M-6DC-2-G1 Cutting shaping bone including spine and cranium.
Reason for recall
G1 Dissection Tools are not compatible with all attachments listed on the labeling; G1 cutting tools are labeled with a Specified Shaft Exposure which may not be consistent when used with each attachment on the product label. Shaft exposure may be greater.
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-2298-2015. 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.