# FDA recall Z-1529-2020

> **Fresenius Medical Care Holdings, Inc.** · Class II · device recall initiated 2020-01-29.

## Product

Honeywell Pressure Transducer- Part Number: 370506-22. It is a component used in 2008T, Common Name: Hemodialysis Delivery System; 2008T HD SYS. BLUE STAR; 2008K2, Common Name: Hemodialysis Delivery Equipment; 2008K@home, Common Name: Hemodialysis Delivery System

## Reason for recall

The firm is replacing pressure transducers with an improved design due to an increase in customer complaints regarding lower long-term reliability of the part.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1529-2020
- **Recalling firm:** Fresenius Medical Care Holdings, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-01-29
- **Report date:** 2020-04-01
- **Termination date:** 2021-01-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waltham, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1529-2020

## Citation

> AI Analytics. FDA recall Z-1529-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1529-2020. Source: US FDA. Licensed CC0.

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