ACCUFIT A282

MAUDE Adverse Event Report

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..

Event Text Entries

[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


MAUDE Entry Details

Report Number1416900-1999-00047
MDR Report Key251279
Report Source00
Date Received1999-11-23
Date of Report1999-10-08
Date of Event1999-10-01
Date Mfgr Received1999-10-08
Device Manufacturer Date1999-08-01
Date Added to Maude1999-11-29
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactDEAN HAYES
Manufacturer Street4201 W. VICTORIA ST.
Manufacturer CityCHICAGO IL 60646
Manufacturer CountryUS
Manufacturer Postal60646
Manufacturer Phone7735833600
Manufacturer G1BELTONE ELECTRONICS CORP.
Manufacturer Street4201 W. VICTORIA ST.
Manufacturer CityCHICAGO IL 60646
Manufacturer CountryUS
Manufacturer Postal Code60646
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameACCUFIT
Generic NameIMPRESSION MATERIAL
Product CodeLDG
Date Received1999-11-23
Model NumberNA
Catalog NumberA282
Lot Number908098
ID NumberNA
Device Expiration Date2000-08-01
OperatorOTHER
Device AvailabilityN
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key243434
ManufacturerBELTONE ELECTRONICS CORP.
Manufacturer Address4201 WEST VICTORIA ST. CHICAGO IL 60646 US
Baseline Brand NameACCUFIT
Baseline Generic NameIMPRESSION MATERIAL
Baseline Model NoNA
Baseline Catalog NoA282
Baseline IDNA
Baseline Device FamilyKIT, EARMOLD IMPRESSION
Baseline Shelf Life ContainedY
Baseline Shelf Life [Months]12
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK963958
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 1999-11-23

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