FDA Adverse Event Injury Summary report: N

COOLSCULPTING SYSTEM

MDR report key: 12602201 · Received October 9, 2021

Report

Report Number
3007215625-2021-01804
Event Type
Injury
Date Received
October 9, 2021
Date of Event
September 20, 2021
Report Date
May 27, 2025
Manufacturer
ALLERGAN PLEASANTON
Product Code
OOK
PMA / PMN Number
-
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER
Health Professional
N

Narratives

Additional Manufacturer Narrative · 0

H11-: CORRECTED DATA: SUBSEQUENT TO THE SUBMISSION OF INITIAL MEDWATCH, THIS REPORT HAS BEEN IDENTIFIED AS A DUPLICATE OF PREVIOUSLY SUBMITTED MEDWATCH REPORT OF 3007215625-2021-01831-00.

Additional Manufacturer Narrative · 0

CORRECTED DATA: B5, D1, D4.

Description of Event or Problem · 0

(B)(6). DUPLICATE OF (B)(6). (B)(6) WILL BE CANCELLED. A PATIENT REPORTED THAT THEY HAD RECEIVED COOLSCULPTING TREATMENT TO THE ABDOMEN ON (B)(6) 2020 AND PRESENTED WITH PAH.

Description of Event or Problem · 0

UPON FURTHER REVIEW OF THE REPORTED EVENT, THIS REPORT HAS BEEN IDENTIFIED AS A DUPLICATE REPORT.

Additional Manufacturer Narrative · 1

ACCORDING TO THE COOLSCULPTING USER MANUAL, UNDER RARE ADVERSE EVENTS, PARADOXICAL ADIPOSE HYPERPLASIA 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. A SUPPLEMENTAL REPORT WILL BE SUBMITTED IF AND WHEN ADDITIONAL INFORMATION IS OBTAINED.

Description of Event or Problem · 1

ALLERGAN AESTHETICS RECEIVED A REPORT OF A PATIENT WHO RECEIVED COOLSCULPTING TREATMENT ON THE ABDOMEN AND PRESENTED WITH PARADOXICAL ADIPOSE HYPERPLASIA.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1500130 COOLSCULPTING SYSTEM DERMAL COOLING PACK/VACUUM/MASSAGER OOK ALLERGAN PLEASANTON NI

Patients

Seq Age Sex Outcome Treatment
1 47 YR Unknown Required Intervention