FDA recall record

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.

Class IIclassification
Z-2192-2025official record ID
Aug 6, 2025report date

Recall record at a glance

Official recordZ-2192-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmPhasor Health, LLC
Report dateAug 6, 2025
Recall initiation dateMar 21, 2025
Quantity1,064
LocationHouston, TX, United States

Official product description

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

Why the product was recalled

Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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