MicroAire Surgical Instruments, LLC recalls ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use.
- Recall date
- June 12, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2822-2015
- FDA classification
- Class II
- Brand / firm
- MicroAire Surgical Instruments, LLC
- Sold / distributed
- Nationwide Distribution.
Why it was recalled
There is potential risk of electrical shock if lead wires inside the device become detached and the ground connection fails.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use.
Get recall alerts
Free email alert whenever MicroAire Surgical Instruments, LLC has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: MicroAire Surgical Instruments, LLC