# FDA recall Z-0724-2022

> **Philips North America Llc** · Class II · device recall initiated 2021-11-24.

## Product

Philips Allura Xper, UNIQ(Allura Xper system-China)  Interventional Fluoroscopic X-ray System products with a Laird chiller WITHOUT an extended drip tray:  Model Number: 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722014, 722015, 722019, 722020, 722022, 722023, 722024, 722025, 722026, 722027, 722029, 722033, 722034, 722036, 722038, 722039.    Allura Xper F010 {C+F). 722003  Allura Xper F010/10 722005  Allura Xper F020 722006  Allura Xper F020/10 and F020/20 722008  Allura Xper F010 722010  Altura Xper F010/10 722011  Allura Xper F020 722012  Allura Xper FD20 biplane 722013  Allura Xper FDlO OR Table 722014  Allura Xper FD20 OR Table 722015  Allura Xper FDl0/10 OR Table 722019  Allura Xper FD20 Biplane OR Table 722020  Allura Xper FD10 OR Table 722022  Allura Xper FD20 OR Table 722023  Allura Xper FD10/10 OR Table 722024  Altura Xper FD20 Biplane OR Table 722025  Allura Xper FD10 722026  Allura Xper  FD10/10 722027  Altura Xper FD20/10 biplane 722029  Allura Xper FD1

## Reason for recall

Due to a leak in the detector cooling system, cooling liquid may leak outside the drip tray of the chiller. If this occurs the liquid may drip onto electrical components in the R cabinet located in the technical room, which could lead to damage to the system and potentially cause thermal events such as a burning odor, smoke or fire.

## Distribution

US Nationwide  Foreign:  Argentina  Austria  Bangladesh  Brazil  Chile  China  Denmark  Dominican Republic  France  Germany  Greece  India  Indonesia  Iran  Israel  Italy  Japan  Korea, Republic of  Malaysia  Mexico  Netherlands  Philippines  Russian Federation  Saudi Arabia  South Africa  Spain  Sri Lanka  Switzerland  Taiwan  Thailand  Turkey  United Kingdom  Virgin Islands (U.S.)

## Key facts

- **Recall number:** Z-0724-2022
- **Recalling firm:** Philips North America Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-11-24
- **Report date:** 2022-03-16

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0724-2022

## Citation

> AI Analytics. FDA recall Z-0724-2022. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-0724-2022. Source: US FDA. Licensed CC0.

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