# FDA recall Z-2972-2024

> **B Braun Medical Inc** · Class I · device recall initiated 2024-08-07.

## Product

Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U

## Reason for recall

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.

## Distribution

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

## Key facts

- **Recall number:** Z-2972-2024
- **Recalling firm:** B Braun Medical Inc
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-07
- **Report date:** 2024-09-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Breinigsville, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2972-2024

## Citation

> AI Analytics. FDA recall Z-2972-2024. Retrieved 2026-06-14 from https://api.ai-analytics.org/recall/Z-2972-2024. Source: US FDA. Licensed CC0.

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