FDA Adverse Event
Other
Summary report: N
HANNAFORD
MDR report key: 3210828
·
Received July 2, 2013
Report
- Report Number
- 1038758-2013-00015
- Event Type
- Other
- Date Received
- July 2, 2013
- Date of Event
- June 11, 2013
- Report Date
- July 2, 2013
- Manufacturer
- ASO LLC
- Product Code
- KGX
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- ME, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Description of Event or Problem · 1
THE END USER COMPLAINED THAT THE BANDAGE TORE HER SKIN WHEN SHE PULLED IT OFF.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 302897 | HANNAFORD | ADHESIVE BANDAGES | KGX | ASO LLC | HBC725434997018 | UNKNOWN |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |