---
title: "Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U — FDA record Z-2972-2024 | Is It on Recall"
description: "Extension of previous recall RES 92978. Pumps have the potential for upstream occlusion sensor to cease proper function due to buildup of electrostatic charge d"
url: https://isitonrecall.com/recall/fda-device-z-2972-2024-infusomat-space-infusion-system-large-volume-pump-product-code-8713050u/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U — FDA record Z-2972-2024

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 Aug 7, 2024. 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**: Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U
- **Reason**: Extension of previous recall RES 92978. Pumps have the potential for upstream occlusion sensor to cease proper function due to buildup of electrostatic charge during operation triggering false downstream and upstream occlusion alarms. Additional devices have been affected.
- **Classification**: Class I
- **Recalling firm**: B Braun Medical Inc
- **Quantity**: 14
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2972-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2972-2024%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 (GUDID) - 04046963716752 Serial Numbers 52226, 107529, 123259, 123815, 123843, 139003, 147678, 147721, 147725, 239018, 239165, 239231, 239279, 339337 |

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

## Distribution

US distribution to AL, CA, GA, IL, MI, and TX.

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

- [Alabama](https://isitonrecall.com/state/alabama/)
- [California](https://isitonrecall.com/state/california/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Michigan](https://isitonrecall.com/state/michigan/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Sep 18, 2024
- **Recall initiation date**: Aug 7, 2024
- **Center classification date**: Sep 6, 2024

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-2972-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [B. Braun Medical, Inc. records](https://isitonrecall.com/brand/b-braun-medical-inc/)