RIEMANN 3 CM NASAL DRESSING RR 300

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2009-12-18 for RIEMANN 3 CM NASAL DRESSING RR 300 manufactured by Arthrocare Corp..

Event Text Entries

[1514237] This physician has been using arthrocare rapid rhino rr 300 products since 2006. For the past two years, however, he has noticed that after removing the device, there have been local, granulating, partly fibrous, alterations in the mucous membrane, some of which have led to membrane decay. In some cases, this has subsequently led to septum perforations. The physician did not provide any info about any one specific incident.
Patient Sequence No: 1, Text Type: D, B5


[8322455] No individual incident date info was provided by the physician, so the date of occurence is approximated as the date of incident on the arthrocare form filled out by the physician. The device is not returning for evaluation. A follow-up report will be completed once a lot history review is completed.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2951580-2009-00129
MDR Report Key1565275
Report Source04
Date Received2009-12-18
Date of Report2009-12-18
Date of Event2009-11-05
Date Added to Maude2011-03-11
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 FDA0
Event Location0
Manufacturer ContactVALERIE DEFIESTA-NG
Manufacturer Street680 VAQUEROS AVE.
Manufacturer CitySUNNYVALE CA 94085
Manufacturer CountryUS
Manufacturer Postal94085
Manufacturer Phone4087360224
Manufacturer G1ARTHROCARE COSTA RICA
Manufacturer CityLA AURORA, HEREDIA
Manufacturer CountryCS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRIEMANN 3 CM NASAL DRESSING
Generic NameGEL KNIT REMOVABLE DRESSINGS
Product CodeEMX
Date Received2009-12-18
Catalog NumberRR 300
Lot Number2007-02 04
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerARTHROCARE CORP.
Manufacturer Address680 VAQUEROS AVE. SUNNYVALE CA 94085 US 94085


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2009-12-18

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.