Class II — Aerolase Corporation
| Recalling firm | AEROLASE CORPORATION |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily available remote interlock connector for the laser device |
| Product | LightPod Neo Lasers |
| Quantity | 649 |
| Distribution | US Nationwide Distribution |
| Initiated | 2019-08-01 |
| Classified | 2020-01-03 |
| Terminated | 2021-03-30 |
| Recall number | Z-0769-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Aerolase Corporation (Z-0769-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/84568/
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