FDAApril 7, 2022device
NanoSight NS300
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Product found to not comply to Class 1 Laser safety requirement.
What to do
FDA enforcement status: Ongoing
Brands named
malvern panalyticalmalvern
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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