Product Wiki · Recalls · U.S. FDA — Device Enforcement

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. — recall Z-1946-2024

U.S. FDA — Device Enforcement · United States · 2024-03-27 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1946-2024
Date of alert
2024-03-27
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Newport Corp
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
23060081
Reported risk: 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.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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