FDA Device recall Z-2192-2025
Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35
- FDA Device
- Class II
- ongoing
- Published 2025-08-06
On 2025-08-06 the FDA classified a Class II recall of Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35 by Phasor Health, citing drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2192-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-03-21 |
| Published | 2025-08-06 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Phasor Health |
| Distribution | AR, AZ, CA, DE, FL, GA, IL, IN, LA, MA, MI, MN, MO, NE, NH, NJ, NY, OH, PA, PR, SC, TN, TX, VA, VT, WA, WI, WV |
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.
Identifiers
| code_info | UDI-DI: B775270S0, B775320L0, B7754500, B7755300, B7756350. Lot: 241002450, 241002530, 241009450, 241009530, 241016450…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. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2192-2025%22
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