Phasor Drill (Phasor Health) – battery orientation risk (2025)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35
Brand
Phasor Health, LLC
Lot Codes / Batch Numbers
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.
Products Sold
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.
Phasor Health, LLC is recalling Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35 due to Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.
Recommended Action
Per FDA guidance
Starting on 3/21/2025, device correction and removal began and a correction and removal notice was emailed. Customers were asked to do the following: 1) Review inventory (without opening the sterile transparent barrier) to determine if any of the affected lots remain in inventory. If yes, remove those lots from inventory. Do not use drills with reverse battery orientation. 2) If unable to review inventory soon, the Company will come to your site within 30 business days of this letter and inspect your inventory (within 20 minutes total) and replace any defective drills with new verified stock (same catalog number). 3) Contact firm at info@phasorhealth.com to report results of inventory inspection and to facilitate device return. 4) Complete and return the acknowledgement and receipt form via email to info@phasorhealth.com Please contact Firm at info@phasorhealth.com or (832) 982-1234 for more information or questions
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, AR, CA, DE, FL, GA, IL, IN, LA, MA, MI, MN, MO, NE, NH, NJ, NY, OH, PA, SC, TN, TX, VT, VA, WA, WV, WI, PR
Page updated: Jan 10, 2026