FDA Adverse Event
Other
Summary report: N
NEUTRALON BROWN STYLE 52
MDR report key: 687262
·
Received March 15, 2006
Report
- Report Number
- 1019632-2006-00001
- Event Type
- Other
- Date Received
- March 15, 2006
- Report Date
- March 15, 2006
- Manufacturer
- ANSELL SHAH ALAM SDN BHD
- Product Code
- KGO
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
PINHOLE IN GLOVE DISCOVERED DURING USE. CUSTOMER COMPLAINS THAT PHYSICIANS WAS ELECTRICALLY SHOCKED WHILE USING GLOVES.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | NEUTRALON BROWN STYLE 52 | SURGICAL GLOVE | KGO | ANSELL SHAH ALAM SDN BHD | * | 0410055321 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Other |