# FDA recall Z-1904-2021

> **Philips Medical Systems Nederlands** · Class II · device recall initiated 2016-06-23.

## Product

Philips Allura Xper System: Interventional Fluoroscopic X-Ray System  Product No.: 722026, 722027, 722028, 722029, 722035, 722038, and 722058.

## Reason for recall

Certain low-voltage DC power supplies (DCPS) used in these products may be subject to an increased probability of failure. Failure of a DCPS may result in the sudden loss of imaging functionality or mechanical movement, depending on what subsystems the DCPS is powering.

## Distribution

Worldwide distribution. US states of: AL, AZ, FL, GA, IL, MA, MO, NJ, OR, and VA;  Netherlands, United Kingdom, Poland, Spain, France, Czech Republic, India, Brazil, Singapore, Japan, Colombia, United Arab Emirates, China, Russian Federation, Oman, and Mexico.

## Key facts

- **Recall number:** Z-1904-2021
- **Recalling firm:** Philips Medical Systems Nederlands
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2016-06-23
- **Report date:** 2021-06-30
- **Termination date:** 2023-02-08

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1904-2021

## Citation

> AI Analytics. FDA recall Z-1904-2021. Retrieved 2026-09-09 from https://api.ai-analytics.org/recall/Z-1904-2021. Source: US FDA. Licensed CC0.

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