Siemens Medical Solutions recalls ACUSON Juniper ultrasound systems with serial numbers 550010-554118. The clip store function may fail when disk full, potentially delaying critical treatment during high-risk procedures like stress echo exams.
The clip store function in the ultrasound imaging system does not work when the system has a disk full error. This could cause a delay in treatment if the ultrasound system is unable to save clips as study documentation during a high risk procedure, such as a stress echo exam.
Siemens is recalling ACUSON Juniper ultrasound systems that may not save clips when the system has a disk full error. This could delay treatment during high-risk procedures like stress echo exams. Affected units have specific serial numbers listed in the recall.
When the ultrasound system's disk becomes full, the clip store function may not work properly. This could prevent the system from saving clips as study documentation during high-risk procedures, potentially delaying critical treatment steps.
Healthcare providers using Siemens ACUSON Juniper ultrasound systems with serial numbers from 550010 to 554118 are most at risk. Patients undergoing high-risk procedures like stress echo exams could experience delays in treatment if the system fails to save clips.
Check if your ACUSON Juniper ultrasound system has a serial number between 550010 and 554118. The system is intended for vascular, abdominal, neonatal, and other medical imaging applications.
Verify if your ACUSON Juniper ultrasound system has a disk full error when attempting to save clips.
Reach out to Siemens Medical Solutions for guidance on potential fixes or alternatives.
The recalled model is Siemens ACUSON Juniper ultrasound system with serial numbers from 550010 to 554118.
The recall states this could delay treatment during high-risk procedures, but it does not indicate a risk of serious injury or death.
Check if your ACUSON Juniper ultrasound system has a serial number between 550010 and 554118.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-0748-2022 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-0748-2022 from Siemens. 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.
