United Nuclear Scientific High Power Handheld Lasers — Class II medical device recall Z-0051-2018
Terminated recall by United Nuclear Scientific Supplies, LLC, reported 2017-12-20. Failure to comply with the laser class limitation listed in the performance standard for Specific Use Laser pr
| Recall number | Z-0051-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA mandated |
| Recalling firm | United Nuclear Scientific Supplies, LLC, East Lansing, MI, United States |
| Recall initiated | 2016-08-25 |
| Classified | 2017-12-08 |
| Reported by FDA | 2017-12-20 |
| Terminated | 2020-10-27 |
| Quantity | 3 |
Product
United Nuclear Scientific High Power Handheld Lasers. Laser products
Reason for recall
Failure to comply with the laser class limitation listed in the performance standard for Specific Use Laser products.
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-0051-2018. 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.