# FDA recall Z-1442-2022

> **MALVERN PANALYTICAL LTD** · Class II · device recall initiated 2022-04-07.

## Product

NanoSight NS300

## Reason for recall

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

## Distribution

US Nationwide - Worldwide Distribution

## Key facts

- **Recall number:** Z-1442-2022
- **Recalling firm:** MALVERN PANALYTICAL LTD
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-04-07
- **Report date:** 2022-08-10

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Malvern, N/A, United Kingdom

## Primary source

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

## Citation

> AI Analytics. FDA recall Z-1442-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1442-2022. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
