Product Safety Recalls

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MALVERN PANALYTICAL LTD Recall 90597

Description: NanoSight NS300

MALVERN PANALYTICAL LTD Recall 90597 Information

StatusOngoing
Mandated?FDA Mandated
Recall NumberZ-1442-2022
Event ID90597
Event DescriptionNanoSight NS300
Product TypeDevices
DistributionUS Nationwide - Worldwide Distribution
Quantity507 units
Recall ReasonProduct found to not comply to Class 1 Laser safety requirement.
Device Classification20220810
Device Code InfoCDRH accession #0510530-003
Center Classification Date20220801
Recall Initiation Date20220407
Recalling FirmMALVERN PANALYTICAL LTD
Initial Notification Letter
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