PlainRecalls
FDA Devices Moderate Class II Ongoing

Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35

Reported: August 6, 2025 Initiated: March 21, 2025 #Z-2192-2025

Product Description

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.

Details

Recalling Firm
Phasor Health, LLC
Units Affected
1,064
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
Location
Houston, TX

Frequently Asked Questions

What product was recalled?
Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35. Recalled by Phasor Health, LLC. Units affected: 1,064.
Why was this product recalled?
Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 6, 2025. Severity: Moderate. Recall number: Z-2192-2025.