FDA Adverse Event Injury Summary report: N

CARDINAL HEALTH

MDR report key: 608266 · Received May 25, 2005

Report

Report Number
608266
Event Type
Injury
Date Received
May 25, 2005
Date of Event
March 30, 2005
Report Date
May 18, 2005
Manufacturer
CARDINAL HEALTH, INC.
Product Code
JCX
Adverse Event
Yes
Product Problem
Yes
Report Source
User Facility report
Reporter Location
FL, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

PHYSICIAN REPORTED THAT PT POST LIPOSUCTION HAD MULTIPLE AREAS OF HARDENED FAT THAT HAD NOT BEEN SUCTIONED OUT. PHYSICIAN NOTED THAT THE SUCTION TUBING KEPT COLLAPSING ON ITSELF. THIS WAS THE CAUSE OF THE FAT NOT BEING SUCTIONED OUT COMPLETELY. HAVE USED THIS SAME TUBING IN THE PAST WITHOUT PROBLEMS. THOUGHT THAT THIS TUBING IS DEFECTIVE. PT WILL NEED TO HAVE SURGERY REDONE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CARDINAL HEALTH SUCTION TUBING JCX CARDINAL HEALTH, INC. * V5B1000

Patients

Seq Age Sex Outcome Treatment
1 61 YR Required Intervention