Ad-Tech Medical Instrument Corporation: Device Recall
Recall #Z-0220-2025 · 09/19/2024
Class II: Risk
Recall Details
- Recall Number
- Z-0220-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Ad-Tech Medical Instrument Corporation
- Status
- Ongoing
- Date Initiated
- 09/19/2024
- Location
- Oak Creek, WI, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 4 units
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.
Product Description
AD-TECH Spencer Probe Depth Electrode, REF SD06R-AP58X-000 6-Contact 1.12mm (A style) Depth Electrode
Distribution Pattern
US Nationwide distribution in the states of CA, OH.
Other Recalls by Ad-Tech Medical Instrument Corporation
- Class II: Risk 09/19/2024
- Class II: Risk 09/19/2024
View all recalls by Ad-Tech Medical Instrument Corporation →
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.