# FDA recall Z-1754-2024

> **SEDECAL SA** · Class II · device recall initiated 2024-01-22.

## Product

Battery Mobile X-ray Unit EASY MOVING Model with telescopic column 3.1, model numbers:    a.  SM-20HF-Batt;  b.  SM-32HF-Batt;  c.  SM-40HF-Batt;  d.  SM-50HF-Batt;  e.  SM-40-HF-B-D-VIR;  f.   SM-20HF-B-D-KM (AeroDR X30);  g.  SM-32-HF-B-D-KM (AeroDR X30);  h.  SM-40HF-B-D-KM (AeroDR X30);  i.   SM-50HF-B-D-KM (AeroDR X30);  j.   MobileDiagnost wDR.

## Reason for recall

Potential interference with the anti-fall system.

## Distribution

Worldwide distribution - US Nationwide in the states of CA, IL, NJ, and areas yet to be identified by Philips Medical Systems DMC GmbH, Hamburg, Germany.

## Key facts

- **Recall number:** Z-1754-2024
- **Recalling firm:** SEDECAL SA
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-01-22
- **Report date:** 2024-05-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Algete, Spain

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1754-2024

## Citation

> AI Analytics. FDA recall Z-1754-2024. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-1754-2024. Source: US FDA. Licensed CC0.

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