---
title: "Digisonics OBView Versions 4.8.2 SP6 - 4.8.3, Ultrasound reporting software — FDA record Z-2214-2023 | Is It on Recall"
description: "Software issue"
url: https://isitonrecall.com/recall/fda-device-z-2214-2023-digisonics-obview-versions-4-8-2-sp6-4-8-3-ultrasound-reporting-software/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Digisonics OBView Versions 4.8.2 SP6 - 4.8.3, Ultrasound reporting software — FDA record Z-2214-2023

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jun 26, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Digisonics OBView Versions 4.8.2 SP6 - 4.8.3, Ultrasound reporting software
- **Reason**: Software issue
- **Classification**: Class II
- **Recalling firm**: Digisonics, Inc
- **Quantity**: 32 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2214-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2214-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI?DI 00857050006014, Versions 4.8.2 SP6 - 4.8.3 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US Distribution: AK, NH, WY, TX, NE, CA, MD, TX, OR IA, IL, MO, OR, NY, UT, PA, MA, GA, VA, WA, WI, and Internationally to :Aruba

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alaska](https://isitonrecall.com/state/alaska/)
- [California](https://isitonrecall.com/state/california/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Iowa](https://isitonrecall.com/state/iowa/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Massachusetts](https://isitonrecall.com/state/massachusetts/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [Missouri](https://isitonrecall.com/state/missouri/)
- [Nebraska](https://isitonrecall.com/state/nebraska/)
- [New Hampshire](https://isitonrecall.com/state/new-hampshire/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Oregon](https://isitonrecall.com/state/oregon/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Utah](https://isitonrecall.com/state/utah/)
- [Virginia](https://isitonrecall.com/state/virginia/)
- [Washington](https://isitonrecall.com/state/washington/)
- [Wisconsin](https://isitonrecall.com/state/wisconsin/)
- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jul 26, 2023
- **Recall initiation date**: Jun 26, 2023
- **Center classification date**: Jul 20, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2214-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Digisonics, Inc records](https://isitonrecall.com/brand/digisonics-inc/)