EBI recalls 20" lead wires (part 1067724-2) sold since May 2023 due to potential wire damage causing treatment delays. Affected devices may not deliver therapeutic signals properly.
Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being delivered to the electrodes, and result in delay of treatment
EBI is recalling 20-inch lead wires with part number 1067724-2 that were sold starting May 1, 2023. The wires can develop damage to their protective sheath, which might prevent proper treatment signals from reaching electrodes and delay medical care.
The lead wire's protective sheath can become damaged, exposing the internal wires. This may cause the device to fail delivering therapeutic signals to the electrodes, potentially delaying treatment.
Patients using EBI's 20-inch lead wires for medical treatments are likely affected. Those with devices distributed since May 1, 2023, are at risk.
Check for the part number 1067724-2 on the wires. Devices were distributed starting May 1, 2023, and have a unique identifier starting with 00812301020300.
Look for the part number 1067724-2 on the wires and the unique identifier starting with 00812301020300.
The part number is 1067724-2.
These wires were distributed starting May 1, 2023.
Check for the part number 1067724-2 and the unique identifier starting with 00812301020300.
We’ve drafted a message you can send EBI to request your refund or repair — edit it as you like.
Subject: Recall Z-1618-2024 — EBI EBI Hello, I own a EBI that is covered by recall Z-1618-2024 from EBI. 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.