Ad-Tech recalls A-Style SD Depth Electrodes with incorrect MR safety labels. These devices may not be safe for MRI use due to misplaced safety symbols.
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 Spencer Probe Depth Electrodes because they have the wrong MRI safety label. Using these devices in MRI machines could cause injury due to improper safety markings.
The electrodes were labeled with an MR Conditional symbol instead of the required MR Unsafe symbol. This means they were not cleared for MRI use, which could lead to injury if used in MRI machines.
Medical professionals using MRI equipment who own the recalled electrodes. Those who use these devices in MRI settings are most at risk.
Check for the model number SD06R-AP58X-000 and lot numbers 169260 or 169258. The product has a UDI/DI code starting with 00841823107589.
Look for the MR Conditional symbol instead of the MR Unsafe symbol on the electrode label.
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 were not cleared for MRI use, which could cause injury if used in MRI machines.
Check for the model number SD06R-AP58X-000 and lot numbers 169260 or 169258. The product has a UDI/DI code starting with 00841823107589.
We’ve drafted a message you can send Ad-Tech to request your refund or repair — edit it as you like.
Subject: Recall Z-0220-2025 — Ad-Tech Ad-Tech Hello, I own a Ad-Tech that is covered by recall Z-0220-2025 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.
