Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2192-2025 — Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35

U.S. FDA — Device Enforcement · United States · 2025-03-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2192-2025
Date of alert
2025-03-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Phasor Health, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
241002450
Reported risk: Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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