---
title: "V-Sign Sensor 2, REF VS-A/P/N, a component of Sentec Digital Monitoring Syste... — FDA record Z-1980-2023 | Is It on Recall"
description: "The sensors may experience an out-of-box failure because after recalibration, the sensors stayed in the software mode \"production\" and were not reset to \"releas"
url: https://isitonrecall.com/recall/fda-device-z-1980-2023-v-sign-sensor-2-ref-vs-a-p-n-a-component-of-sentec-digital-monitoring-system-model-sdms/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# V-Sign Sensor 2, REF VS-A/P/N, a component of Sentec Digital Monitoring System (model SDMS). — FDA record Z-1980-2023

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 May 2, 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**: V-Sign Sensor 2, REF VS-A/P/N, a component of Sentec Digital Monitoring System (model SDMS).
- **Reason**: The sensors may experience an out-of-box failure because after recalibration, the sensors stayed in the software mode "production" and were not reset to "released" mode.
- **Classification**: Class II
- **Recalling firm**: SenTec AG
- **Quantity**: 11 in the U.S.
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1980-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1980-2023%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 | Serial numbers 338947, 338952, 338953, 338963, 338967, 338989, 338991, 338993, 338994, 338996, 338997, UDI-DI 07640121880513. |

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

## Distribution

US Nationwide distribution in the states of CA, FL, IL, MA, MS, MT, NV, and TX.

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

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## Dates in the source

- **Report date**: Jun 28, 2023
- **Recall initiation date**: May 2, 2023
- **Center classification date**: Jun 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-1980-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [SenTec AG records](https://isitonrecall.com/brand/sentec-ag/)
