FDA Adverse Event
Injury
Summary report: N
CVS
MDR report key: 4975925
·
Received August 4, 2015
Report
- Report Number
- 1038758-2015-00060
- Event Type
- Injury
- Date Received
- August 4, 2015
- Report Date
- August 4, 2015
- Manufacturer
- ASO LLC
- Product Code
- KGX
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- RI, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
THE CONSUMER HAS NOT PROVIDED SAMPLES OF THE DEVICE OR THE LOT NUMBER.
Description of Event or Problem · 1
ON (B)(6) 2015 - THE END USER REPORTED THAT THE END ITEM RIPPED OFF SOME SKIN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 509319 | CVS | ADHESIVE BANDAGE | KGX | ASO LLC | UPC 050428120620 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |