Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35 recall — FDA Z-2192-2025
Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.
Overview of recall records associated with Phasor Health, LLC, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.
This page summarizes recall records in which the official source identifies Phasor Health, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.