FDA Device recall Z-1442-2022
NanoSight NS300
- FDA Device
- Class II
- ongoing
- Published 2022-08-10
On 2022-08-10 the FDA classified a Class II recall of NanoSight NS300 by Malvern Panalytical, citing product found to not comply to Class 1 Laser safety requirement.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1442-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-04-07 |
| Published | 2022-08-10 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Malvern Panalytical |
| Distribution | US |
Product
NanoSight NS300
Reason
Product found to not comply to Class 1 Laser safety requirement.
Identifiers
| code_info | CDRH accession #0510530-003 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1442-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.