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 |