# FDA recall Z-1823-2025

> **Maquet Cardiopulmonary Ag** · Class II · device recall initiated 2025-04-30.

## Product

Cardiohelp System HKH 8820 Wall Holder. Mounting bracket designed to hold the CARDIOHELP-i system for interhospital transport by vehicle.

## Reason for recall

HKH 8820 Wall Holder does not comply with standard DIN EN 1789:20 and has the potential to detach.

## Distribution

Domestic: IL & MO. Foreign: Australia, Austria, Belgium, Canada, China, Colombia, Croatia, Czech Republic, Denmark, Finland, France, Germany, India, Israel, Italy, Japan, South Korea, Poland, Russia, Saudi Arabia, Spain, Switzerland, Thailand.

## Key facts

- **Recall number:** Z-1823-2025
- **Recalling firm:** Maquet Cardiopulmonary Ag
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-04-30
- **Report date:** 2025-06-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Rastatt, N/A, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1823-2025

## Citation

> AI Analytics. FDA recall Z-1823-2025. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-1823-2025. Source: US FDA. Licensed CC0.

---

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