MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00 report with the FDA on 1999-11-23 for ACCUFIT A282 manufactured by Beltone Electronics Corp..
[20240396]
The hearing aid (h/a) dispenser reported an incidnet of difficulty of removing accufit impression material from a h/a pt's ear. Upon removal, there was bleeding in the concha. The bleeding was stopped with a tissue. The h/a pt was referred to her doctor.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1416900-1999-00047 |
MDR Report Key | 251279 |
Report Source | 00 |
Date Received | 1999-11-23 |
Date of Report | 1999-10-08 |
Date of Event | 1999-10-01 |
Date Mfgr Received | 1999-10-08 |
Device Manufacturer Date | 1999-08-01 |
Date Added to Maude | 1999-11-29 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 0 |
Manufacturer Contact | DEAN HAYES |
Manufacturer Street | 4201 W. VICTORIA ST. |
Manufacturer City | CHICAGO IL 60646 |
Manufacturer Country | US |
Manufacturer Postal | 60646 |
Manufacturer Phone | 7735833600 |
Manufacturer G1 | BELTONE ELECTRONICS CORP. |
Manufacturer Street | 4201 W. VICTORIA ST. |
Manufacturer City | CHICAGO IL 60646 |
Manufacturer Country | US |
Manufacturer Postal Code | 60646 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ACCUFIT |
Generic Name | IMPRESSION MATERIAL |
Product Code | LDG |
Date Received | 1999-11-23 |
Model Number | NA |
Catalog Number | A282 |
Lot Number | 908098 |
ID Number | NA |
Device Expiration Date | 2000-08-01 |
Operator | OTHER |
Device Availability | N |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 243434 |
Manufacturer | BELTONE ELECTRONICS CORP. |
Manufacturer Address | 4201 WEST VICTORIA ST. CHICAGO IL 60646 US |
Baseline Brand Name | ACCUFIT |
Baseline Generic Name | IMPRESSION MATERIAL |
Baseline Model No | NA |
Baseline Catalog No | A282 |
Baseline ID | NA |
Baseline Device Family | KIT, EARMOLD IMPRESSION |
Baseline Shelf Life Contained | Y |
Baseline Shelf Life [Months] | 12 |
Baseline PMA Flag | N |
Baseline 510K PMN | Y |
Premarket Notification | K963958 |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 1999-11-23 |