Esaote recalls specific batch of E 3-12 endocavity ultrasonic probes (UDI 0805604453891) due to potential liquid leakage from the probe casing. Affected units may leak liquid near the cable connection.
A potential weakness has been identified in the probe body, so that, in a specific production batch, liquid may leak from the terminal part of the casing near the cable.
Esaote is recalling a specific batch of E 3-12 ultrasonic probes because liquid could leak from the casing near the cable. This could cause electrical issues or damage if the probe is used in medical procedures.
The probe has a potential weakness in the casing that could allow liquid to leak from the terminal part near the cable. This leakage might cause electrical short circuits or damage to medical equipment during procedures.
Medical professionals using the Esaote E 3-12 ultrasonic probe with the specific serial numbers or UDI mentioned in the recall. Patients undergoing procedures with this probe may be at risk if liquid leaks.
Check for the UDI code 0805604453891 or serial numbers 241700533C, 241700529C, 241700607C, 241700536C, or 241700613C on the probe's label.
Look for the UDI code 0805604453891 or the listed serial numbers on the probe's label.
This recall specifically affects Esaote E 3-12 ultrasonic probes with the UDI 0805604453891 and the listed serial numbers. If your probe has these identifiers, it is affected.
The recall does not specify a remedy, so you should check with Esaote directly to determine if you need to take action.
The recall states a potential liquid leak but does not mention risk of serious injury. The hazard level is low risk as per the official notice.
We’ve drafted a message you can send Esaote to request your refund or repair — edit it as you like.
Subject: Recall Z-1490-2026 — Esaote Esaote Hello, I own a Esaote that is covered by recall Z-1490-2026 from Esaote. 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.
