# FDA recall Z-0221-2025

> **Ad-Tech Medical Instrument Corporation** · Class II · device recall initiated 2024-09-19.

## Product

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

## Reason for recall

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.

## Distribution

US Nationwide distribution in the states of CA, OH.

## Key facts

- **Recall number:** Z-0221-2025
- **Recalling firm:** Ad-Tech Medical Instrument Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2024-09-19
- **Report date:** 2024-10-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Oak Creek, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0221-2025

## Citation

> AI Analytics. FDA recall Z-0221-2025. Retrieved 2026-07-08 from https://api.ai-analytics.org/recall/Z-0221-2025. Source: US FDA. Licensed CC0.

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