# FDA recall Z-0872-2022

> **B Braun Medical Inc** · Class II · device recall initiated 2022-01-28.

## Product

Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis  Systems. Conductivity Sensor (BIC) - VERSION 2, Article Code Number 3456102A. These conductivity sensors may be used as spare parts for the following dialysis machines: 710200L (UDI 04046963686345), 710200S  (UDI 04046964285608), 710200U (UDI 04046964285615), 710200K (UDI 04046963686338), 710500L (UDI Not  applicable) and 710500K (UDI Not applicable).

## Reason for recall

Firm learned of the potential for cracks to form in the conductivity sensors during use, which may lead to a leak in the dialysate circuit. This could result in excessive ultrafiltration or insufficient ultrafiltration depending on whether the dialysis machine is equipped with a Dialysis Fluid filter.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-0872-2022
- **Recalling firm:** B Braun Medical Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-01-28
- **Report date:** 2022-04-20
- **Termination date:** 2024-05-15

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0872-2022

## Citation

> AI Analytics. FDA recall Z-0872-2022. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-0872-2022. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*