FDA Device recall Z-1693-2023
p-Chip Wand Reader
- FDA Device
- Class II
- ongoing
- Published 2023-06-21
On 2023-06-21 the FDA classified a Class II recall of p-Chip Wand Reader by P Chip, citing the laser operation might fall under a higher laser class.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1693-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-03-03 |
| Published | 2023-06-21 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | P Chip |
| Distribution | US |
Product
p-Chip Wand Reader
Reason
The laser operation might fall under a higher laser class.
Identifiers
| code_info | Model: WA-4000, 4500, -8000, and -8500 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1693-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.