FDA Adverse Event
Injury
Summary report: N
PRO-PICC - MAXIMUM BARRIER KIT
MDR report key: 8624659
·
Received May 17, 2019
Report
- Report Number
- MW5086758
- Event Type
- Injury
- Date Received
- May 17, 2019
- Date of Event
- May 2, 2019
- Report Date
- May 15, 2019
- Manufacturer
- MEDCOMP (MEDICAL COMPONENTS, INC.)
- Product Code
- LJS
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- FL, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
ON (B)(6) 2019 PICC LINE NOTED TO HAVE CRACKED HUB. LINE REMOVED. FDA SAFETY REPORT ID# (B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 411832 | PRO-PICC - MAXIMUM BARRIER KIT | CATHETER, INTRAVASCULAR THERAPEUTIC LONG TERM GREATER THAN 30 DAYS | LJS | MEDCOMP (MEDICAL COMPONENTS, INC.) | MR170235206MB | MMAT250 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 68 YR | Required Intervention |