FDA Adverse Event
Other
Summary report: N
PREMIUM WET TRAY - LATEX-FREE
MDR report key: 491497
·
Received October 16, 2003
Report
- Report Number
- 1417592-2003-00030
- Event Type
- Other
- Date Received
- October 16, 2003
- Date of Event
- December 3, 2002
- Report Date
- October 16, 2003
- Manufacturer
- MEDLINE INDUSTRIES, INC.
- Product Code
- LRO
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
REPORTEDLY A PT RECEIVED A SKIN INJURY POTENTIALLY RELATED TO CONTACT WITH POVIDONE IODINE SOLUTION. THE PT REQUIRED WOUND CARE TREATMENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PREMIUM WET TRAY - LATEX-FREE | POVIDONE IODINE IN WET TRAY | LRO | MEDLINE INDUSTRIES, INC. | DYND70660 | 02AC00011 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Other |