Class 2 Device Recall Sedecal Easy Moving Plus

• Date Initiated by Firm: June 10, 2025
• Date Posted: October 23, 2025
• Recall Status: Open, Classified
• Recall Number: Z-0277-2026
• Recall Event ID: 97075
• 510(K)Number: K090322
• Product Classification: System, x-ray, mobile - Product Code IZL
• Product: Model Number SM-40HF-B-D-C; 40KW, Mobile X-ray system
• Code Information: UDI/DI 08436046001510, Serial Numbers: G65281, G60407, G65682, G64582, G64789, G70752, G65384, G65418, G67250, G68470, G70521, G70524, G70913, G70914, G65166, G63507, G64205, G64842, G71447, G65175, G65382, G64793, G64798, G40226, G72434, G65554, G67230, G37280, G65174, G65558, 15033R, G64271, G64713, G64849, G65168, G71272, G71309, G65284, G72955, G65043, G70919, G72429, G72789, G70928, G72776, G72766, G63409, G63418, G64893, G66907, G65588, G65402, G73096, G73131, G71269, G71750, G71762, G71267, G71727, G71732, G71745, G71755, G71761, G66892, G65275, G70922, G73154, G64505, G65744, G73033, G73134, G64941, G63489, G65036, G64256, G72976, G73092, G73145, G64196, G64945, G72412, G73074, G65414, G71726, G71743, G64807, G66872, G67257, G40208, G64885, G38391, G39467, G39818, G65408, G70748, G37108, G6715, G67232, G71277, G71286, G64604, G37406, G40004, G63223, G63224, G63232, G61711, G71271, G71302, G72790, G64500, G65269, G65692, G65290, G65691, G66862, G65283, G64189, G70744, G64812, G70755, G65286, G65266, G72760, G66884, G64601, G71300, G67185, G63495, G64890, G72780, G64607, G63488, G63494, G71285 - NCR1161, G63501, G41245, G64797, G64819, G64855, G72803, G41213.
• FEI Number: 3002495042
• Recalling Firm/ Manufacturer: SEDECAL SA; Pelaya, 9 Pol.; Pol. Ind. Rio De Janeiro; Algete Spain
• For Additional Information Contact: Marie Luisa Gomez de Aguero; 8473946960
• Manufacturer 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.
• FDA Determined Cause: Device Design
• Action: Sedecal emailed their distributors on 06/10/2025 to remind them 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. on 09/19/2025 the firm issued an Important Safety Notice to its direct consignees via email. This notice initiates Phase 2 of the recall strategy expanding the scope and providing information on stickers to cover gaps around the fine positioning control buttons and a DMC software update that stops unit movement if triggered by a short cicuit or prolonged button press with instructions. Consignees will be contacted by a Sedecal Customer support Service to coordinate the shipment of the necessary conversion kits (quantity and delivery address) to allow upgrading the affected units.
• Quantity in Commerce: 142 units
• Distribution: US: CA, IL, and NJ
• Total Product Life Cycle: TPLC Device Report

¹ A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
² Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
³ The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.

• 510(K) Database: 510(K)s with Product Code = IZL