YXL:ON Cougar cabinet X-ray systems may fail to disconnect power when door opens, risking electrical hazards. Affected units were sold for non-destructive testing. Contact manufacturer for details.
Failure to meet the requirement of the performance standard for cabinet x-ray systems (21 CFR 1020.40) for a door interlock that causes physical disconnection of the power supply using only the movement of the door.
YXLON Cougar cabinet X-ray systems are being recalled because their door interlock may fail to disconnect power when opened, creating an electrical hazard. This could lead to electric shock or fire if the system is used without proper safety measures.
The door interlock mechanism may fail to disconnect the power supply when the cabinet door is opened. This could allow electrical current to flow during operation, potentially causing electric shock or fire if the system is not properly secured.
Users of YXLON Cougar cabinet X-ray systems for non-destructive testing and quality control are affected. Those operating these systems in industrial or laboratory settings are most at risk.
Check for YXLON Cougar cabinet X-ray systems used in non-destructive testing. The product was sold for industrial and quality control applications. Specific model numbers are not listed in the recall notice.
Ensure the door interlock disconnects power when opened by testing the system. If it fails, stop using the system immediately.
The door interlock may fail to disconnect power when the cabinet door opens, creating an electrical hazard.
The recall notice does not specify a remedy or action steps for affected users.
The recall states the hazard could lead to electric shock or fire, but does not specify the likelihood of serious injury.
We’ve drafted a message you can send YXLON to request your refund or repair — edit it as you like.
Subject: Recall Z-2106-2019 — YXLON YXLON Hello, I own a YXLON that is covered by recall Z-2106-2019 from YXLON. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
