FDA Adverse Event Injury Summary report: N

COOLSCULPTING SYSTEM

MDR report key: 15651915 · Received October 21, 2022

Report

Report Number
3007215625-2022-01584
Event Type
Injury
Date Received
October 21, 2022
Date of Event
October 10, 2021
Report Date
December 6, 2023
Manufacturer
ALLERGAN PLEASANTON
Product Code
OOK
PMA / PMN Number
K160259
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TC
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

ACCORDING TO THE COOLSCULPTING USER MANUAL, UNDER RARE ADVERSE EVENTS, PARADOXICAL ADIPOSE HYPERPLASIA (PH/PAH) IS CHARACTERIZED BY A VISIBLY ENLARGED TISSUE VOLUME WITHIN THE TREATMENT AREA, WHICH MAY DEVELOP TWO TO FIVE MONTHS AFTER TREATMENT. SURGICAL INTERVENTION MAY BE REQUIRED. PAH IS NOT RELATED TO ANY COOLSCULPTING DEVICE FAILURE MODE BUT IT IS OBSERVED MORE FREQUENTLY WITH THE PARALLEL PLATE APPLICATORS. PAH IS INCLUDED IN THE RISK MANAGEMENT FILES OF THE DEVICE AS AN INHERENT RISK TO THE USE OF CRYOLIPOLYSIS FOR LOCALIZED FAT REDUCTION. A SUPPLEMENTAL REPORT WILL BE SUBMITTED IF AND WHEN ADDITIONAL INFORMATION IS OBTAINED.

Additional Manufacturer Narrative · 0

H11 - CORRECTED DATA: D1.

Description of Event or Problem · 0

ALLERGAN AESTHETICS RECEIVED A REPORT OF A PATIENT TREATED SUBMENTAL ON (B)(6) 2021 WITH COOLSCULPTING COOLMINI DEVELOPED PARADOXICAL HYPERPLASIA (PAH/PH). DIAGNOSED WITH PAH ON (B)(6) 2022 BY MEDICAL DOCTOR.

Description of Event or Problem · 0

ALLERGAN AESTHETICS RECEIVED A REPORT OF A PATIENT TREATED SUBMENTAL ON (B)(6) 2021 WITH COOLSCULPTING COOLMINI DEVELOPED PARADOXICAL HYPERPLASIA (PAH/PH). DIAGNOSED WITH PAH ON (B)(6) 2022 BY MEDICAL DOCTOR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2022088 COOLSCULPTING SYSTEM DERMAL COOLING PACK/VACUUM/MASSAGER OOK ALLERGAN PLEASANTON NI

Patients

Seq Age Sex Outcome Treatment
1 22 YR Female Required Intervention