Phasor Drill — Class II medical device recall Z-2192-2025
Ongoing recall by Phasor Health, LLC, reported 2025-08-06, distributed in AR, AZ, CA, DE, FL, GA, GU, IL…. Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical
| Recall number | Z-2192-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Phasor Health, LLC, Houston, TX, United States |
| Recall initiated | 2025-03-21 |
| Classified | 2025-07-29 |
| Reported by FDA | 2025-08-06 |
| Distributed | AR, AZ, CA, DE, FL, GA, GU, IL, IN, LA, MA, MI, MN, MO, NE, NH, NJ, NY, OH, PA, PR, SC, TN, TX, VA, VT, WA, WI, WV |
| Quantity | 1,064 |
| Lot numbers | 24082832L, 241002450, 241002530, 241009450, 241009530, 241016450, 241016530, 24102332L, 241023450, 241023530, 241030450, 241030530, 24112027S, 24121827S, 241220635, 24122727S, 241227450, 241227530, 25012227S, 250122530, 250122635 |
| Model numbers | 2.70S, 3.20L, 4.50, 5.30, 6.35 |
Product
Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35
Reason for recall
Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2192-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.