Anspach G1 High Speed Electric Handpiece Air Cooled — Class II medical device recall Z-2253-2016
Terminated recall by The Anspach Effort, Inc., reported 2016-07-27, distributed in FL, GA. The graphics at the attachment interface indicating locked and unlocked position are reversed.
| Recall number | Z-2253-2016 |
|---|---|
| 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 | 2016-06-15 |
| Classified | 2016-07-21 |
| Reported by FDA | 2016-07-27 |
| Terminated | 2016-12-14 |
| Distributed | FL, GA |
| Countries outside the US | CH |
| Quantity | 18 |
| Lot numbers | H29309439804, H44310033104, K09311396703, K09311396704 |
Product
Anspach G1 High Speed Electric Handpiece Air Cooled (eG1A) Use for cutting and shaping bone including bones of the cranium and spine.
Reason for recall
The graphics at the attachment interface indicating locked and unlocked position are reversed.
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-2253-2016. 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.