YXLON recalls Cheetah cabinet X-Ray systems due to door interlock failure that could disconnect power. Products used for non-destructive testing may pose safety risks if door movement causes power loss.
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.
YXL:ON is recalling its Cheetah cabinet X-Ray systems because a door interlock failure could disconnect power when the door is opened. This risk could lead to unsafe conditions during non-destructive testing and quality control operations.
The door interlock system fails to meet safety standards, meaning opening the cabinet could disconnect the power supply. This creates a risk of unexpected power loss during operation, which could cause equipment malfunction or safety hazards in industrial environments.
Users of YXLON Cheetah cabinet X-Ray systems for non-destructive testing and quality control are affected. Those operating these systems in industrial settings face the highest risk due to potential power disconnection during door movement.
Check for YXLON Cheetah cabinet X-Ray systems used in non-destructive testing and quality control. The specific model and serial numbers are not provided in the recall notice.
Ensure the door interlock system maintains power connection when opened during operation.
The recall applies to YXLON Cheetah cabinet X-Ray systems used for non-destructive testing and quality control. Specific model numbers are not listed in the notice.
The recall notice does not specify a remedy or action steps for affected users.
The recall states the hazard could disconnect power during door movement, but does not specify injury risks or severity.
We’ve drafted a message you can send YXLON to request your refund or repair — edit it as you like.
Subject: Recall Z-2105-2019 — YXLON YXLON Hello, I own a YXLON that is covered by recall Z-2105-2019 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.
