# FDA recall Z-0874-2022

> **Philips North America Llc** · Class II · device recall initiated 2022-02-02.

## Product

Philips Allura (Model Numbers 722010, 722012, 722026, 722027, 722028, 722029, 722035) and Philips Azurion (Model Numbers 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222, 722223, 722224, 722225, 722226, 722227, 722228) running StentBoost Live (Model Number 459801781661) Software Version Number: R2.0

## Reason for recall

Due to a software defect, the Philips StentBoost Live R2.0 might not process X-ray images of the current run and instead show an image processed in a previous run. The image shown could be from the same patient or from a different patient.

## Distribution

Global Distribution.  US Nationwide.

## Key facts

- **Recall number:** Z-0874-2022
- **Recalling firm:** Philips North America Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-02-02
- **Report date:** 2022-04-13

- **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-0874-2022

## Citation

> AI Analytics. FDA recall Z-0874-2022. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-0874-2022. Source: US FDA. Licensed CC0.

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