Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1761-2022 — NanoSight LM10 fitted with LM12 module. A laboratory instrument for determination of particle characteristics (e.g. size).

U.S. FDA — Device Enforcement · United Kingdom · 2022-02-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1761-2022
Date of alert
2022-02-28
Country / jurisdiction
United Kingdom
Risk level
Class II
Risk type
recall
Brand
MALVERN PANALYTICAL LTD
Product category
device
Product type
Devices
Reported risk: Product found to not comply to Class 1 Laser safety requirement.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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