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Terminated

YXLON Cheetah cabinet X-Ray System Product Usage: The products are generally used for non-destructive testing and quality control

FDA Recall Z-2105-2019 · Posted None

Recalling FirmComet Technologies Usa Inc
Recall StatusTerminated
Product CodeRCE
Date Initiated2018-10-01
Date Terminated2024-06-13
Product Quantity77

Reason for Recall

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.

Firm Action

The firm sent a notification letter dated July 2019, to affected customers. The letter identified the affected products, problem and actions to be taken. Customers were informed that a service technician will be contacting you to schedule the retrofit service. For questions, call YXLON Service at (234) 284-7881.

Root Cause

Radiation Control for Health and Safety Act

Distribution Pattern

US Nationwide Distribution

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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