FDA Adverse Event
Injury
Summary report: N
PICC LINE
MDR report key: 4190261
·
Received October 13, 2014
Report
- Report Number
- MW5038688
- Event Type
- Injury
- Date Received
- October 13, 2014
- Date of Event
- September 2, 2014
- Report Date
- October 13, 2014
- Manufacturer
- BARD
- Product Code
- LJS
- Report Source
- Voluntary report
- Reporter Location
- US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Description of Event or Problem · 1
NEW PICC LINE PLACED AND NEEDED REPOSITIONED. DURING REPOSITIONING, GUIDEWIRE WAS RETAINED IN PATIENT'S ARM. PATIENT WENT TO (B)(6) THE NEXT DAY FOR SAFE REMOVAL OF THE RETAINED GUIDEWIRE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 647206 | PICC LINE | PICC LINE | LJS | BARD | REYG0688 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 43 YR | Required Intervention |