SEDECAL SA: Device Recall

Recall #Z-0243-2026 · 06/10/2025

Class II: Risk

Recall Details

Recall Number
Z-0243-2026
Classification
Class II
Product Type
Device
Recalling Firm
SEDECAL SA
Status
Ongoing
Date Initiated
06/10/2025
Location
Algete, Spain
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1198 units

Reason for Recall

Sedecal sent an email to its consignees to remind the users that the equipment is not water-resistant and must be cleaned strictly according to the instructions in the manual, clearly outlining the possible consequences of improper cleaning.

Product Description

MobileDiagnost wDR 2.2; Model Number REF 9890-010-89522, Mobile X-ray system

Distribution Pattern

US: CA, IL, and NJ

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.