G1 Dissection Tool — Class II medical device recall Z-2838-2016
Terminated recall by The Anspach Effort, Inc., reported 2016-09-28, distributed in AZ, CA, DC, MD, MI, OR. The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.
| Recall number | Z-2838-2016 |
|---|---|
| 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 | 2016-08-26 |
| Classified | 2016-09-16 |
| Reported by FDA | 2016-09-28 |
| Terminated | 2017-11-29 |
| Distributed | AZ, CA, DC, MD, MI, OR |
| Countries outside the US | CH |
| Quantity | 88 |
| Lot numbers | J313108568, J316017637 |
Product
G1 Dissection Tool - 3mm CRS DBALL, 2mm SHAFT EXP, M; For cutting and shaping bone including spine and cranium.
Reason for recall
The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.
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-2838-2016. 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.