MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2006-10-23 for THE FIRST YEARS FLOATING FRIENDS * manufactured by *.
[20024296]
"the first years" teething ring broke and child consumed liquid. Used 2 mos.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1040772 |
| MDR Report Key | 772830 |
| Date Received | 2006-10-23 |
| Date of Report | 2006-10-23 |
| Date Added to Maude | 2006-10-26 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | THE FIRST YEARS FLOATING FRIENDS |
| Generic Name | TEETHER |
| Product Code | KKO |
| Date Received | 2006-10-23 |
| Model Number | FLOATING FRIENDS |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Device Availability | Y |
| Device Age | * |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 760612 |
| Manufacturer | * |
| Manufacturer Address | * * * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2006-10-23 |