Class II — Phasor Health, LLC
| Recalling firm | Phasor Health, LLC |
|---|---|
| Registered facility | PHASOR HEALTH, LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time. |
| Product | Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35 |
| Quantity | 1,064 |
| Distribution | US: PA, IN, AZ, MO, LA, FL, TX, MA, OH, TN, MI, WV, VA, CA, DE, NH, GA, SC, GU, NY, NJ, MN, WI, NE, WA, IL, AR, PR, VT |
| Initiated | 2025-03-21 |
| Classified | 2025-07-29 |
| Recall number | Z-2192-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Phasor Health, LLC (Z-2192-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/97089/
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