Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Newport s N-LHP-928(j) units if sold as a laser head/power supply set Recalled by Newport Corp Due to According to 21 CFR 1040.10(f)(4), each laser system...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Newport Corp directly.
Affected Products
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.
Quantity: 19
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Newport Corp
Newport Corp has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report