# FDA recall Z-0311-2018

> **Philips Electronics North  America Corporation** · Class II · device recall initiated 2017-07-14.

## Product

Mobile Detector Holder - Stationary X-ray System (RF System). suitable for positioning the wireless portable detector free in the room for X-ray exposures. It supports the wireless portable detector with or without a grid.

## Reason for recall

If the lock mechanism of the movable camp of the mobile detector holder is not adjusted properly or not secured, the portable detector can drop down when the moveable clamp is at the bottom (below of the detector) and additional force is applied. This may happen when the detector is rotated clockwise from landscape to portrait position.

## Distribution

412 units affected.

## Key facts

- **Recall number:** Z-0311-2018
- **Recalling firm:** Philips Electronics North  America Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-07-14
- **Report date:** 2018-01-10
- **Termination date:** 2020-06-05

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0311-2018

## Citation

> AI Analytics. FDA recall Z-0311-2018. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0311-2018. Source: US FDA. Licensed CC0.

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