Houston, TX, United States
Phasor Health, LLC recalls
1 recall recorded since 2018, most recently on 21 March 2025. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 21 March 2025
- Reason
- Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.
- 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
- Voluntary: Firm initiated
- Recall number
- Z-2192-2025
- Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.