FDA Device recall Z-2253-2016
Anspach G1 High Speed Electric Handpiece Air Cooled (eG1A) Use for cutting and shaping bone including bones of the cranium and spine
- FDA Device
- Class II
- terminated
- Published 2016-07-27
On 2016-07-27 the FDA classified a Class II recall of Anspach G1 High Speed Electric Handpiece Air Cooled (eG1A) Use for cutting and shaping bone including bones of the cranium and spine by The Anspach Effort, citing the graphics at the attachment interface indicating locked and unlocked position are reversed.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2253-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-06-15 |
| Published | 2016-07-27 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | The Anspach Effort |
| Distribution | FL, GA |
Product
Anspach G1 High Speed Electric Handpiece Air Cooled (eG1A) Use for cutting and shaping bone including bones of the cranium and spine.
Reason
The graphics at the attachment interface indicating locked and unlocked position are reversed.
Identifiers
| code_info | Lot #'s: H29309439804, H44310033104, K09311396703, and K09311396704. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2253-2016%22
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