FDAMarch 27, 2024device

Newport s N-LHP-928(j) units if sold as a laser head/power supply set, and N5-LPL-944-080 and N6-LPL-944-080 if sold as a power supply alone.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

According to 21 CFR 1040.10(f)(4), each laser system classified as a Class IIIb or IV laser product shall incorporate a key-actuated master control. The key shall be removable and the laser shall not be operable when the key is removed. However, the key of the subject laser products can be removed from key switch and the laser remains on. This is a safety concern.

What to do

FDA enforcement status: Ongoing

Brands named

newport

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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