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FDA (Device enforcement)Recalled 2024-03-01class ii

PACIFIC LASERTECH, LLC: 25-LHP-928, HeNe Laser System, 25 mW

Hazard

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.

Details from the source

Reason for recall: 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. Distribution: US Nationwide Distribution Quantity: 4 Lot/code info: 25-LHP-928

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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