FDA recall Z-1693-2023

p-Chip Corporation · Class II · device

Product

p-Chip Wand Reader

Reason for recall

The laser operation might fall under a higher laser class.

Distribution

US Nationwide Distribution

Key facts

Status
Ongoing
Initiation date
2021-03-03
Report date
2023-06-21
Voluntary/Mandated
FDA Mandated
Location
Chicago, IL, United States

Primary source

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