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Open, Classified

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FDA Recall Z-2416-2024 · Posted 2024-07-26

Recall StatusOpen, Classified
Product CodeRIB
Date Initiated2024-07-22

Reason for Recall

A broken fuse inside the laser that was caused by a short circuit at PIN 4 of the DOOR CTRL. This short circuit was caused by a badly positioned cable that made contact with the housing/frame and caused a short circuit and destroyed the fuse in the laser. This caused the shutter to remain in its most recent state; either in an open or closed position. Once the fuse was destroyed the shutter could not be operated.

Root Cause

Radiation Control for Health and Safety Act

Distribution Pattern

US

Official Source

View FDA Recall →

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

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