# FDA recall Z-0070-2026

> **B BRAUN MEDICAL INC** · Class I · device recall initiated 2025-09-30.

## Product

Brand Name: Hemodialysis Bloodlines  Product Name: STREAMLINE BLOODLINE SET FOR DIALOG  Model/Catalog Number: SL-2010M2096  Software Version: N/A  Product Description: STREAMLINE BLOODLINE SET FOR DIALOG  Component: N/A

## Reason for recall

The potential for micro-air bubbles observed in the bloodline and air-in-line alarms due to damaged arterial and venous patient connectors.

## Distribution

Domestic: US Nationwide Distribution.

## Key facts

- **Recall number:** Z-0070-2026
- **Recalling firm:** B BRAUN MEDICAL INC
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-09-30
- **Report date:** 2025-10-29

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0070-2026

## Citation

> AI Analytics. FDA recall Z-0070-2026. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-0070-2026. Source: US FDA. Licensed CC0.

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