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

Recall Z-0221-2025 — AD-TECH Spencer Probe Depth Electrode, REF SD08R-AP58X-000 8-Contact 1.12mm (A style) Depth Electrode

U.S. FDA — Device Enforcement · United States · 2024-09-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0221-2025
Date of alert
2024-09-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ad-Tech Medical Instrument Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00841823107688
Reported risk: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label discrepancy was identified on A style contact SD electrodes where the MR Conditional symbol was incorrectly placed instead of the MR Unsafe symbol. The A style contacts were not cleared for MR Conditional use. Our records indicate you have received one or more of the affected lots listed above.
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.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.