Recall Z-1442-2022— MALVERN PANALYTICAL LTD

Name: FDA recall Z-1442-2022
Creator: U.S. Food and Drug Administration
Published: 2022-04-07

Class II · Ongoing

Class II FDA medical device recall by MALVERN PANALYTICAL LTD, initiated 2022-04-07. FDA's recall record names no specific 510(k) clearance for this event. Product: NanoSight NS300. Reason: Product found to not comply to Class 1 Laser safety requirement..

Recalling firm: MALVERN PANALYTICAL LTD
Classification: Class II
Status: Ongoing
Initiated: 2022-04-07
Firm location: Malvern, N/A, United Kingdom

Product description

NanoSight NS300

Reason for recall

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.