Data Foundry

Medical device recalls 2024

Battery Mobile X-ray Unit EASY MOVING Model with telescopic column 3 — Class II medical device recall Z-1754-2024

Ongoing recall by SEDECAL SA, reported 2024-05-08, distributed nationwide. Potential interference with the anti-fall system.

Recall numberZ-1754-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmSEDECAL SA, Algete, Spain
Recall initiated2024-01-22
Classified2024-05-02
Reported by FDA2024-05-08
DistributedNationwide (US)
Countries outside the USDE
Quantity636 devices
UPC / GTIN / UDI-DI08436046001497, 08436046001503, 08436046001510, 08436046001527, 08436046002166, 08436046002357, 08436046002579, 08436046002586, 08436046002593, 08436046002609
Model numbers3.1, SM-20HF-BATT

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1754-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.