ClearanceBrief
Recall Z-0243-2026 ยท IZL System, X-Ray, Mobile

SEDECAL SA

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

DateOct 23, 2025 (initiated Jun 10, 2025)
StatusOpen, Classified
ReasonSedecal 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.
Root causeDevice Design
ActionSedecal 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 cicui
Quantity1198 units
DistributionUS: CA, IL, and NJ
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K111725MOBILEDIAGNOST WDR
Sedecal., Sa., Jul 19, 2011
K141895MOBILEDIAGNOST WDR
Sedecal., Sa., Sep 18, 2014
K191813MobileDiagnost wDR 2.2
Sedecal., Sa., Aug 2, 2019