RAPTAR Laser Range Finders — Class II medical device recall Z-0001-2022
Ongoing recall by Potomac River Group, Corp., reported 2021-11-03, distributed nationwide. RAPTAR units are capable of being field modified to enable the use of the higher power visible and IR laser po
| Recall number | Z-0001-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Potomac River Group, Corp., Ashburn, VA, United States |
| Recall initiated | 2021-04-21 |
| Classified | 2021-10-22 |
| Reported by FDA | 2021-11-03 |
| Distributed | Nationwide (US) |
| Quantity | 62 units |
| Model numbers | 57200G02 |
Product
RAPTAR Laser Range Finders
Reason for recall
RAPTAR units are capable of being field modified to enable the use of the higher power visible and IR laser pointers and the IR Illuminator.
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-0001-2022. 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.