ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump — Class II medical device recall Z-2822-2015
Terminated recall by MicroAire Surgical Instruments, LLC, reported 2015-10-07, distributed nationwide. There is potential risk of electrical shock if lead wires inside the device become detached and the ground con
| Recall number | Z-2822-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | MicroAire Surgical Instruments, LLC, Charlottesville, VA, United States |
| Recall initiated | 2015-06-12 |
| Classified | 2015-09-30 |
| Reported by FDA | 2015-10-07 |
| Terminated | 2016-05-23 |
| Distributed | Nationwide (US) |
| Reason classes | device malfunction |
| Serial numbers | 12101105, 12101106, 12101107, 12111108, 12121109, 12121111, 12121112, 13011113, 13021114, 13021116, 13021118, 13021120, 13031121, 13031122, 13031123, 13041124, 13041125, 13041126, 13041127, 13041128, 13041129, 13041130, 13041131, 13051132, 13051133 and 144 more |
Product
ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use.
Reason for recall
There is potential risk of electrical shock if lead wires inside the device become detached and the ground connection fails.
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-2822-2015. 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.