# FDA recall Z-1693-2023

> **p-Chip Corporation** · Class II · device recall initiated 2021-03-03.

## Product

p-Chip Wand Reader

## Reason for recall

The laser operation might fall under a higher laser class.

## Distribution

US Nationwide Distribution

## Key facts

- **Recall number:** Z-1693-2023
- **Recalling firm:** p-Chip Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-03-03
- **Report date:** 2023-06-21

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Chicago, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1693-2023

## Citation

> AI Analytics. FDA recall Z-1693-2023. Retrieved 2026-07-06 from https://api.ai-analytics.org/recall/Z-1693-2023. Source: US FDA. Licensed CC0.

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