Drug recall
Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35
FDA recall event 97089 · Class II · Phasor Health, LLC
Key facts
| Event ID | 97089 |
|---|---|
| Recall numbers | Z-2192-2025 |
| Recalling firm | Phasor Health, LLC |
| Product type | Devices |
| Products | Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time. |
| Initiation date | Mar 21, 2025 |
| Report date | Aug 6, 2025 |
| City | Houston |
| State | TX |
| Country | United States |
| FEI number | 3016577622 |
At a glance
- 1–9 Products in this recall
- None 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: