AD-TECH Spencer Probe Depth Electrode — Class II medical device recall Z-0220-2025
Completed recall by Ad-Tech Medical Instrument Corporation, reported 2024-10-30, distributed nationwide. Ad-Tech is recalling these A-Style SD Depth Electrodes because a label discrepancy was identified on A style c
| Recall number | Z-0220-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ad-Tech Medical Instrument Corporation, Oak Creek, WI, United States |
| Recall initiated | 2024-09-19 |
| Classified | 2024-10-24 |
| Reported by FDA | 2024-10-30 |
| Distributed | Nationwide (US) |
| Quantity | 4 units |
| Reason classes | labeling, unapproved product |
| UPC / GTIN / UDI-DI | 00841823107589 |
| Lot numbers | 169258, 169260, 858859860 |
| Model numbers | 1.12MM, 6-CONTACT, D06R-AP58X-000 |
Product
AD-TECH Spencer Probe Depth Electrode, REF SD06R-AP58X-000 6-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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0220-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.