FDA Adverse Event
Malfunction
Summary report: N
APOTHECON
MDR report key: 39449
·
Received September 24, 1996
Report
- Report Number
- MW4001508
- Event Type
- Malfunction
- Date Received
- September 24, 1996
- Date of Event
- August 29, 1996
- Report Date
- August 29, 1996
- Manufacturer
- BRISTOL-MYERS SQUIBB
- Product Code
- LNW
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- IN, US
- Reporter Occupation
- PHARMACIST
Narratives
Description of Event or Problem · 1
NITRAZINE PAPER DISPENSER WAS PICKED UP TO USE. ENTIRE CONTENTS WERE LIGHT GREEN (PH APPROX 5.5). TAPE USUALLY COMES BRIGHT YELLOW FROM MFR. NOT AWARE OF ANY EXPOSURE TO ALKALI OR ACID FUMES. PRODUCT RETURNED TO PHARMACY NOT USED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | APOTHECON | NITRAZINE PAPER | LNW | BRISTOL-MYERS SQUIBB | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Other |