EBI recalls 48" lead wires (part 1067724-4) sold since May 2023. Damaged sheath may cause treatment delays. Contact for replacement.
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 48-inch lead wires sold since May 2023 because damage to the cable sheath could cause treatment delays. This affects medical devices used for therapeutic treatments.
The lead wire's protective sheath can become damaged, exposing the wires. This may prevent the device from delivering treatment signals properly, causing delays in therapy.
Patients using medical devices that require these lead wires are affected. Those with devices installed since May 2023 are most at risk.
Check for part number 1067724-4 on the wire. Devices were sold starting May 1, 2023. The wires are 48 inches long.
Look for part number 1067724-4 on the 48-inch lead wires. Devices were sold starting May 1, 2023.
Damage to the lead wire sheath can cause treatment delays by preventing proper signal delivery to electrodes.
The recall record does not specify a remedy, so contact EBI directly for guidance.
These wires were sold starting May 1, 2023.
We’ve drafted a message you can send EBI to request your refund or repair — edit it as you like.
Subject: Recall Z-1619-2024 — EBI EBI Hello, I own a EBI that is covered by recall Z-1619-2024 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.
