Z-2821-2015Class II

ASP-1020 LipoTower with Aspiration Pump. Medical use

Name: Z-2821-2015 ASP-1020 LipoTower with Aspiration Pump. Medical use
Creator: MicroAire Surgical Instruments, LLC
Published: 2015-06-12
License: https://open.fda.gov/license/

MicroAire Surgical Instruments, LLC / initiated 2015-06-12 / Terminated / root cause: design

FDA source

MicroAire Surgical Instruments, LLC began a recall of ASP-1020 LipoTower with Aspiration Pump. Medical use on 2015-06-12. FDA classified it as Class II and gives the reason as "There is potential risk of electrical shock if lead wires inside the device become detached and the ground connection fails". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-2821-2015
Classification: Class II
Status: Terminated
Initiated: 2015-06-12
Posted: 2015-09-30
Terminated: 2016-05-23
Recalling firm: MicroAire Surgical Instruments, LLC
Product: ASP-1020 LipoTower with Aspiration Pump. Medical use.
Product code: MUU System, Suction, Lipoplasty
Reason for recall: There is potential risk of electrical shock if lead wires inside the device become detached and the ground connection fails.
Root cause tag: design
FDA root cause: Device Design
Action: The firm has issued FDA recall letters to all consignees. The letter have been sent out by UPS to expedite the delivery.
Quantity in commerce: 3 LipoTower with Aspiration Pump
Distribution: Nationwide Distribution.
Product codes and lots: Serial numbers 14031102, 15021105, and 14101103.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2821-2015
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2821-2015	Class II	Terminated	Voluntary: Firm initiated	2015-10-07	2015-09-30
Z-2822-2015	Class II	Terminated	Voluntary: Firm initiated	2015-10-07	2015-09-30

Product code MUU

K113128Class IIMicroaire Surgical Instruments LlcMicroaire Surgical Instruments, LLC / cleared 2012-08-17

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)