p-Chip Wand Reader — Class II medical device recall Z-1693-2023
Ongoing recall by p-Chip Corporation, reported 2023-06-21, distributed nationwide. The laser operation might fall under a higher laser class.
| Recall number | Z-1693-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | FDA mandated |
| Recalling firm | p-Chip Corporation, Chicago, IL, United States |
| Recall initiated | 2021-03-03 |
| Classified | 2023-06-12 |
| Reported by FDA | 2023-06-21 |
| Distributed | Nationwide (US) |
| Quantity | 329 units |
| Model numbers | 4500, 8000, 8500, WA-4000 |
Product
p-Chip Wand Reader
Reason for recall
The laser operation might fall under a higher laser class.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1693-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.