# FDA recall Z-1897-2024

> **PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.** · Class II · device recall initiated 2024-05-16.

## Product

Philips Allura Xper FD20 Biplane system with an ADN7NT patient table.  Model Number: 722013, Software Version Number 8.1.100.

## Reason for recall

When Software upgrade 8.1.100 is installed on an Allura Xper with an AD7NT (non tilt) table, the pivot brake does not engage. This issue may cause unexpected movements of the table.

## Distribution

Domestic: OK  International: India, Spain, U.A.E.

## Key facts

- **Recall number:** Z-1897-2024
- **Recalling firm:** PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-05-16
- **Report date:** 2024-06-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Best, Netherlands

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1897-2024

## Citation

> AI Analytics. FDA recall Z-1897-2024. Retrieved 2026-07-08 from https://api.ai-analytics.org/recall/Z-1897-2024. Source: US FDA. Licensed CC0.

---

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