FDA Device recall Z-2821-2015
ASP-1020 LipoTower with Aspiration Pump
- FDA Device
- Class II
- terminated
- Published 2015-10-07
On 2015-10-07 the FDA classified a Class II recall of ASP-1020 LipoTower with Aspiration Pump by Microaire Surgical Instruments, citing there is potential risk of electrical shock if lead wires inside the device become detached and the ground connection fails.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2821-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-06-12 |
| Published | 2015-10-07 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Microaire Surgical Instruments |
| Distribution | US |
Product
ASP-1020 LipoTower with Aspiration Pump. Medical use.
Reason
There is potential risk of electrical shock if lead wires inside the device become detached and the ground connection fails.
Identifiers
| code_info | Serial numbers 14031102, 15021105, and 14101103. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2821-2015%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.