Class II — MicroAire Surgical Instruments, LLC
| Recalling firm | MICROAIRE SURGICAL INSTRUMENTS, LLC |
|---|---|
| Registered facility | MICROAIRE SURGICAL INSTRUMENTS LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | There is potential risk of electrical shock if lead wires inside the device become detached and the ground connection fails. |
| Product | ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use. |
| Quantity | 168, ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump |
| Distribution | Nationwide Distribution. |
| Initiated | 2015-06-12 |
| Classified | 2015-09-30 |
| Terminated | 2016-05-23 |
| Recall number | Z-2822-2015 |
| 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 — MicroAire Surgical Instruments, LLC (Z-2822-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/72106/
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