Digisonics recalls OBView ultrasound reporting software versions 4.8.2 SP6 through 4.8.3 due to a software issue. Affected users should contact Digisonics for details.
Software issue
Digisonics is recalling specific versions of its OBView ultrasound reporting software because of a software issue. This could affect healthcare providers using the software for prenatal ultrasounds.
The software issue could lead to incorrect ultrasound reporting results if not properly addressed. This might impact patient care during prenatal examinations.
Healthcare providers using Digisonics OBView software versions 4.8.2 SP6 through 4.8.3 for prenatal ultrasounds are likely affected. Medical staff handling these versions face the highest risk.
Check if you have Digisonics OBView software versions 4.8.2 SP6 through 4.8.3. The specific UDI?DI number 00857050006014 may also help identify affected units.
Reach out to Digisonics directly for guidance on the recall and next steps.
Digisonics OBView versions 4.8.2 SP6 through 4.8.3.
Look for the software version number 4.8.2 SP6 through 4.8.3 on your system or check the UDI?DI number 00857050006014.
Contact Digisonics directly for instructions on the recall and next steps.
We’ve drafted a message you can send Digisonics to request your refund or repair — edit it as you like.
Subject: Recall Z-2214-2023 — Digisonics Digisonics Hello, I own a Digisonics that is covered by recall Z-2214-2023 from Digisonics. 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.
