FDA Adverse Event
Other
Summary report: N
L-CATH
MDR report key: 11359
·
Received February 7, 1994
Report
- Report Number
- MW1000661
- Event Type
- Other
- Date Received
- February 7, 1994
- Manufacturer
- LUTHER MEDICAL PRODUCTS, INC.
- Product Code
- DQO
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Location
- MO, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
ON 12/20 PICC WAS PLACED. ON 12/25 PICC WAS REMOVED. DR FEELS PT'S ARM PROBLEM IS DUE TO CELLULITIS FROM INSECT BITE, ETC. HOWEVER, RPTR WANTS TO CHECK ABOUT WHY CATH TURNED RED. (NURSES AT DR'S OFFICE HAD GIVEN ADRIAMYCIN.) RPTR WANTED TO MAKE SURE DRUG HADN'T LEAKED OUT SLOWLY EXPLAINING GOOD BLOOD RETURN. ARM PROBLEM DEPENDENT TO VEIN AS IF TOTALLY UNRELATED OR DUE TO GRAVITY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | L-CATH | DQO | LUTHER MEDICAL PRODUCTS, INC. | TRAY PE PIC 03A | LMP1392, LMP 1455 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 52 YR | Other |