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 |