FDA Device recall Z-0051-2018
United Nuclear Scientific High Power Handheld Lasers
- FDA Device
- Class II
- terminated
- Published 2017-12-20
On 2017-12-20 the FDA classified a Class II recall of United Nuclear Scientific High Power Handheld Lasers by United Nuclear Scientific Supplies, citing failure to comply with the laser class limitation listed in the performance standard for Specific Use Laser products.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0051-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-08-25 |
| Published | 2017-12-20 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | United Nuclear Scientific Supplies |
| Distribution | n/a |
Product
United Nuclear Scientific High Power Handheld Lasers. Laser products
Reason
Failure to comply with the laser class limitation listed in the performance standard for Specific Use Laser products.
Identifiers
| code_info | Surveying Leveling and Alignment (SLA) laser products |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0051-2018%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.