MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2004-08-24 for * manufactured by Unk.
[344174]
Pt is allergic to perfumes and many cosmetic products labeled as fragrance free are improperly labeled. Pt just purchased a rubber nasal aspirator and it is so perfumed that pt is unable to use it. Pt asks if nasal aspirator should be perfumed. Pt read in a parents magazine that in children, perfumes are the underlying cause of many ear infections.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW4003818 |
| MDR Report Key | 563242 |
| Date Received | 2004-08-24 |
| Date of Report | 2004-08-16 |
| Date Added to Maude | 2005-01-06 |
| 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 | 0 |
| Report to FDA | 0 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | NA |
| Generic Name | NASAL ASPIRATOR |
| Product Code | LRQ |
| Date Received | 2004-08-24 |
| Model Number | * |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Device Availability | * |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 552970 |
| Manufacturer | UNK |
| Manufacturer Address | UNK UNK * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2004-08-24 |