FDA Adverse Event Injury Summary report: N

UNKNOWN COOLSCULPTING SYSTEM

MDR report key: 11916443 · Received June 1, 2021

Report

Report Number
3007215625-2021-01338
Event Type
Injury
Date Received
June 1, 2021
Date of Event
May 4, 2021
Report Date
May 13, 2024
Manufacturer
ALLERGAN PLEASANTON
Product Code
OOK
PMA / PMN Number
K160259
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IA, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

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 3007215625-2021-01331-00.

Additional Manufacturer Narrative · 0

SUBSEQUENT TO THE SUBMISSION OF INITIAL MEDWATCH, THIS REPORT HAS BEEN IDENTIFIED AS A DUPLICATE OF PREVIOUSLY SUBMITTED MEDWATCH REPORT OF 3007215625-2021-01331-00.

Description of Event or Problem · 0

CASE DUPLICATE TO (B)(4). A COOLSCULPTING TREATMENT PROVIDER REPORTED THAT A PATIENT RECEIVED COOLSCULPTING TREATMENT TO THE LOWER ABDOMEN ON 03/04/2019 AND STARTED EXPERIENCING PARADOXICAL ADIPOSE HYPERPLASIA.

Additional Manufacturer Narrative · 1

THE FOLLOWING INFORMATION IS IN THE COOLSCULPTING USER MANUAL: PARADOXICAL 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. INVESTIGATION IS ONGOING.

Description of Event or Problem · 1

A COOLSCULPTING TREATMENT PROVIDER REPORTED THAT A PATIENT RECEIVED COOLSCULPTING TREATMENT TO THE LOWER ABDOMEN AND FLANKS ON (B)(6) 2019 AND HAS DEVELOPED PARADOXICAL HYPERPLASIA.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
811064 UNKNOWN COOLSCULPTING SYSTEM DERMAL COOLING PACK/VACUUM/MASSAGER OOK ALLERGAN PLEASANTON NI

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention