# FDA recall Z-0273-2024

> **Philips North America Llc** · Class II · device recall initiated 2023-09-21.

## Product

DigitalDiagnost 4 Flex/Value, used to acquire, process, store, display and export digital radiographic images.

## Reason for recall

Potential for units suspended on the ceiling to fail and fall.

## Distribution

Nationwide distribution.

## Key facts

- **Recall number:** Z-0273-2024
- **Recalling firm:** Philips North America Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-21
- **Report date:** 2023-11-15

- **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-0273-2024

## Citation

> AI Analytics. FDA recall Z-0273-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0273-2024. Source: US FDA. Licensed CC0.

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