Ad-Tech recalls A-Style SD depth electrodes with incorrect MR safety labels. These devices may not be safe for MRI use, risking injury during scans. Affected units have specific lot numbers.
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.
Ad-Tech is recalling certain A-Style depth electrodes due to a label error where the MR Conditional symbol was mistakenly placed instead of the MR Unsafe symbol. This means the electrodes are not cleared for MRI use and could cause injury during scans.
The electrodes were labeled as MR Conditional when they should be MR Unsafe. This means they could cause serious injury or death during MRI scans because they are not safe for magnetic resonance imaging procedures.
Medical professionals using MRI machines with these electrodes are most at risk. Patients undergoing MRI scans with these devices could face injury.
Check for the model number SD08R-AP58X-000 on the device. Affected units include lot numbers 168788, 855856857, 172999, 873874875R, and 174915, 879880881.
Look for the model number SD08R-AP58X-000 on the device.
Ad-Tech identified a label discrepancy where the MR Conditional symbol was incorrectly placed instead of the MR Unsafe symbol on A-Style SD depth electrodes.
These electrodes are not cleared for MRI use and could cause injury during scans if used incorrectly.
Check for the model number SD08R-AP58X-000 and lot numbers 168788, 855856857, 172999, 873874875R, or 174915, 879880881.
We’ve drafted a message you can send Ad-Tech to request your refund or repair — edit it as you like.
Subject: Recall Z-0221-2025 — Ad-Tech Ad-Tech Hello, I own a Ad-Tech that is covered by recall Z-0221-2025 from Ad-Tech. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
