FDA Enforcement Class II Ongoing

Model Number 40KWFXPLUS.005, Mobile X-ray system

Recall: Z-0249-2026 · Reported October 29, 2025

Enforcement

Recall Number
Z-0249-2026
Event ID
97075
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
SEDECAL SA
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
October 29, 2025
Initiation Date
June 10, 2025
Classification Date
October 23, 2025
Address
Pelaya, 9 Pol., Pol. Ind. Rio De Janeiro, Algete, N/A, Spain

Description

Model Number 40KWFXPLUS.005, Mobile X-ray system

Reason

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.

Code Info

UDI/DI 08436046002166, Serial Numbers: G82576, G82871, G72391, G74872, G75722, G76782, G75035, G75723, G78884, G70532, G73630, G82077.

Distribution

US: CA, IL, and NJ

Quantity

12 units