Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

REVOLVE ADVANCED ADIPOSE SYSTEM Recalled by LifeCell Corporation, A Wholly Owned Subsidiary of Allergan PLC Due to Presence of bacterial endotoxins levels above the acceptable...

Date: August 8, 2017
Company: LifeCell Corporation, A Wholly Owned Subsidiary of Allergan PLC
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact LifeCell Corporation, A Wholly Owned Subsidiary of Allergan PLC directly.

Affected Products

REVOLVE ADVANCED ADIPOSE SYSTEM, for aspiration, harvesting, filtering, and transferring of autologous adipose tissue for aesthetic body contouring.

Quantity: 25,798 units

Why Was This Recalled?

Presence of bacterial endotoxins levels above the acceptable limit

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About LifeCell Corporation, A Wholly Owned Subsidiary of Allergan PLC

LifeCell Corporation, A Wholly Owned Subsidiary of Allergan PLC has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report