Reported Jul 20, 2022 · Ongoing

CoolFit ZELTIQ Vacuum Applicator REF BRZ-AP1-066-000

Zeltiq Aesthetics, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Zeltiq Aesthetics, Inc · 4410 Rosewood Dr · Pleasanton, CA · 94588-3050

Is this the product you have?

  • CoolFit ZELTIQ Vacuum Applicator REF BRZ-AP1-066-000
Lot codes and dates
  • CoolCurve REFBRZ-AP1-066-000 BRZ-AP1-064-000_R
  • UDI-DI00816417020216
  • Serial Numbers

    2,168 of 2,168 codes

    • V0662016146015
    • V0662016146014
    • V0662016146010
    • V0662016146007
    • V0662016146002
    • V0662016145016
    • V0662016145015
    • V0662016145010
    • V0662016145009
    • V0662016145008
    • V0662016145005
    • V0662016145004
    • V0662016145002
    • V0662016144019
    • V0662016144017
    • V0662016144016
    • V0662016144015
    • V0662016144014
    • V0662016144012
    • V0662016144009
    • V0662016144007
    • V0662016144003
    • V0662016140038
    • V0662016140037
    • V0662016140036
    • V0662016140035
    • V0662016140033
    • V0662016140032
    • V0662016140031
    • V0662016140030
    • V0662016140029
    • V0662016140028
    • V0662016140027
    • V0662016140024
    • V0662016140023
    • V0662016140021
    • V0662016140020
    • V0662016140018
    • V0662016140017
    • V0662016140014
    • V0662016140013
    • V0662016140011
    • V0662016140009
    • V0662016140007
    • V0662016140004
    • V0662016140003
    • V0662016140002
    • V0662016140001
    • V0662016137020
    • V0662016137019
    • V0662016137018
    • V0662016137016
    • V0662016137015
    • V0662016137014
    • V0662016137013
    • V0662016137012
    • V0662016137011
    • V0662016137010
    • V0662016137008
    • V0662016137006
Amount recalled
2,684 units

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

Why it was recalled

Executing a voluntary discontinuation and removal of parallel plate applicators due to an increase complaint rate for adverse event Paradoxical Hyperplasia (HP) during the 2019 to 2021 timeframe.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:37 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.