DERMACEA 441601

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-11-29 for DERMACEA 441601 manufactured by Covidien.

Event Text Entries

[93457897] Submit date: 11/14/2017. An investigation is currently under way; upon completion the results will be forwarded. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[93457898] The customer reported that the sponges were severely linting.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3008361498-2017-05564
MDR Report Key7068592
Date Received2017-11-29
Date of Report2018-02-27
Date Mfgr Received2017-11-03
Date Added to Maude2017-11-29
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactEDWARD ALMEIDA
Manufacturer Street15 HAMPSHIRE STREET
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone5084524151
Manufacturer G1COVIDIEN
Manufacturer Street15 HAMPSHIRE ST.
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal Code02048
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameDERMACEA
Generic NameGAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE
Product CodeNAB
Date Received2017-11-29
Model Number441601
Catalog Number441601
Lot Number17063008
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer Address15 HAMPSHIRE ST. MANSFIELD MA 02048 US 02048


Patients

Patient NumberTreatmentOutcomeDate
10 2017-11-29

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