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Terminated

ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use.

FDA Recall Z-2822-2015 · Posted 2015-09-30

Recalling FirmMicroAire Surgical Instruments, LLC
Recall StatusTerminated
Product CodeMUU
Date Initiated2015-06-12
Date Terminated2016-05-23
Product Quantity168, ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump

Reason for Recall

There is potential risk of electrical shock if lead wires inside the device become detached and the ground connection fails.

Firm Action

The firm has issued FDA recall letters to all consignees. The letter have been sent out by UPS to expedite the delivery.

Root Cause

Device Design

Distribution Pattern

Nationwide Distribution.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K113128MICROAIRE SURGICAL INSTRUMENTS LLCMicroaire Surgical Instruments, LLC · 2012-08-17

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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