Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
25-LHP-928 Recalled by PACIFIC LASERTECH, LLC Due to These laser products fail to comply with 21...
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 PACIFIC LASERTECH, LLC directly.
Affected Products
25-LHP-928, HeNe Laser System, 25 mW
Quantity: 4
Why Was This Recalled?
These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control which requires, 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. , because while the laser is switched on, the key can be removed from the key switch. The correction is replacement with a key switch that captures the key when in the on position.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About PACIFIC LASERTECH, LLC
PACIFIC LASERTECH, LLC has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report