DEROYAL COVARDERM PLUS VAD DRESSING * 46-405

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2000-02-25 for DEROYAL COVARDERM PLUS VAD DRESSING * 46-405 manufactured by Deroyal Industries, Inc..

Event Text Entries

[205346] While removing the dressing, it causes the first layer of the skin to tear. This altered skin integrity.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1123071-2000-00006
MDR Report Key265242
Report Source06
Date Received2000-02-25
Date of Report2000-02-21
Report Date2000-02-21
Date Reported to FDA2000-02-21
Date Mfgr Received2000-01-26
Device Manufacturer Date1999-12-01
Date Added to Maude2000-02-29
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 Location3
Manufacturer Street200 DEBUSK LN
Manufacturer CityPOWELL TN 37849
Manufacturer CountryUS
Manufacturer Postal37849
Manufacturer Phone8659387828
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameDEROYAL COVARDERM PLUS VAD DRESSING
Generic NameWOUND DRESSING
Product CodeMSA
Date Received2000-02-25
Returned To Mfg2000-02-01
Model Number*
Catalog Number46-405
Lot Number289980
ID Number*
Device Expiration Date2004-12-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Age1 MO
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key256782
ManufacturerDEROYAL INDUSTRIES, INC.
Manufacturer Address200 DEBUSK LANE POWELL TN 37849 US
Baseline Brand NameDEROYAL COVADERM PLUS VAD DRESSING
Baseline Generic NameWOUND DRESSING
Baseline Model NoNA
Baseline Catalog No46-405
Baseline IDNA
Baseline Device FamilyWOUND DRESSING
Baseline Shelf Life ContainedY
Baseline Shelf Life [Months]60
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK910657
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2000-02-25

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