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 |