FDA Adverse Event Injury Summary report: N

UNKNOWN COOLSCULPTING SYSTEM

MDR report key: 11996535 · Received June 14, 2021

Report

Report Number
3007215625-2021-01384
Event Type
Injury
Date Received
June 14, 2021
Date of Event
May 24, 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
KS, 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 3007215625-2021-01384-00.

Additional Manufacturer Narrative · 0

IN SECTION H10. CORRECTED STATEMENT IS THE FOLLOWING : SUBSEQUENT TO THE SUBMISSION OF INITIAL MEDWATCH, THIS REPORT HAS BEEN IDENTIFIED AS A DUPLICATE OF PREVIOUSLY SUBMITTED MEDWATCH REPORT OF 3007215625-2021-01434-00.

Description of Event or Problem · 0

A VOICEMAIL WAS LEFT FROM A PROVIDER REPORTING A PATIENT HAS DEVELOPED PARADOXICAL HYPERPLASIA.

Description of Event or Problem · 0

A VOICEMAIL WAS LEFT FROM A PROVIDER REPORTING A PATIENT HAS DEVELOPED PARADOXICAL 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

ALLERGAN RECEIVED A REPORT OF A PATIENT WHO WAS TREATED WITH COOLSCULPTING AND HAS DEVELOPED PARADOXICAL HYPERPLASIA.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
885869 UNKNOWN COOLSCULPTING SYSTEM DERMAL COOLING PACK/VACUUM/MASSAGER OOK ALLERGAN PLEASANTON NI

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention