AQUACEL FOAM 420621

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2019-05-02 for AQUACEL FOAM 420621 manufactured by Convatec Inc.

Event Text Entries

[143841364] (b)(6). Based on the available information, this event is deemed to be a reportable malfunction. To date no additional information has been received. Should additional information become available, a follow-up report will be submitted. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[143841365] It was reported? Black spot on the dressing.? A photograph depicting the reported complaint issue was provided by the complainant.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1049092-2019-00189
MDR Report Key8573872
Report SourceDISTRIBUTOR,FOREIGN
Date Received2019-05-02
Date Mfgr Received2019-04-14
Date Added to Maude2019-05-02
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 ContactMS. JEANETTE JOHNSON
Manufacturer Street211 AMERICAN AVENUE
Manufacturer CityGREENSBORO NC 27409
Manufacturer CountryUS
Manufacturer Postal27409
Manufacturer Phone3365424681
Manufacturer G1CONVATEC INC
Manufacturer Street211 AMERICAN AVENUE
Manufacturer CityGREENSBORO NC 27409
Manufacturer CountryUS
Manufacturer Postal Code27409
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAQUACEL FOAM
Generic NameDRESSING,WOUND,HYDROPHILIC
Product CodeNAC
Date Received2019-05-02
Model Number420621
Lot Number2630386
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCONVATEC INC
Manufacturer Address211 AMERICAN AVENUE GREENSBORO NC 27409 US 27409


Patients

Patient NumberTreatmentOutcomeDate
10 2019-05-02

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