Phasor Health, LLC: Device Recall
Recall #Z-2192-2025 · 03/21/2025
Class II: Risk
Recall Details
- Recall Number
- Z-2192-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Phasor Health, LLC
- Status
- Ongoing
- Date Initiated
- 03/21/2025
- Location
- Houston, TX, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,064
Reason for Recall
Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.
Product Description
Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35
Distribution Pattern
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
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.