Drug recall
Anspach G1 High Speed Electric Handpiece Air Cooled (eG1A) Use for cutting and shaping bone including bones of…
FDA recall event 74447 · Class II · The Anspach Effort, Inc.
Key facts
| Event ID | 74447 |
|---|---|
| Recall numbers | Z-2253-2016 |
| Recalling firm | The Anspach Effort, Inc. |
| Product type | Devices |
| Products | Anspach G1 High Speed Electric Handpiece Air Cooled (eG1A) Use for cutting and shaping bone including bones of the cranium and spine. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The graphics at the attachment interface indicating locked and unlocked position are reversed. |
| Initiation date | Jun 15, 2016 |
| Report date | Jul 27, 2016 |
| Termination date | Dec 14, 2016 |
| City | Palm Beach Gardens |
| State | FL |
| Country | United States |
| FEI number | 1045834 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: