Recall archive / FDA device enforcement
Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35 — FDA record Z-2192-2025
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Mar 21, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35
- Reason
- Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.
- Classification
- Class II
- Recalling firm
- Phasor Health, LLC
- Quantity
- 1,064
- Agency-reported status
- Ongoing
- Source record identifier
- Z-2192-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI-DI: B775270S0, B775320L0, B7754500, B7755300, B7756350. Lot: 241002450, 241002530, 241009450, 241009530, 241016450, 241016530, 241023450, 241023530, 241030450, 241030530, 24112027S, 24121827S, 24122727S, 25012227S, 24082832L, 24102332L, 241227450, 241220635, 250122635, 241227530, 250122530. |
Match all identifying details in the current notice. A brand name alone is not enough.
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
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Aug 6, 2025
- Recall initiation date
- Mar 21, 2025
- Center classification date
- Jul 29, 2025
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.