FDA recall Z-1442-2022

MALVERN PANALYTICAL LTD · Class II · device

Product

NanoSight NS300

Reason for recall

Product found to not comply to Class 1 Laser safety requirement.

Distribution

US Nationwide - Worldwide Distribution

Key facts

Status
Ongoing
Initiation date
2022-04-07
Report date
2022-08-10
Voluntary/Mandated
FDA Mandated
Location
Malvern, N/A, United Kingdom

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1442-2022