DEROYAL A131067

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 2013-07-18 for DEROYAL A131067 manufactured by Deroyal Guatemala.

Event Text Entries

[3609989] The end user reported that after a c-section the pt had an allergic reaction to the abdominal binder. Pt had to use benadryll cream on affected area.
Patient Sequence No: 1, Text Type: D, B5


[10963188] Describe event or problem: the end user reported that after a c-section the pt had an allergic reaction to the abdominal binder. Pt had to use benadryl cream on affected area. Deroyal: the bill of material for the components of the product was reviewed and no material changes to the components were identified for the lot number reported. The product does not contain natural rubber latex.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3005225477-2013-00010
MDR Report Key3246700
Report Source00
Date Received2013-07-18
Date of Report2012-08-22
Date of Event2012-08-22
Date Facility Aware2012-08-22
Report Date2012-08-22
Date Reported to Mfgr2012-08-22
Device Manufacturer Date2012-04-01
Date Added to Maude2013-07-31
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 G1DEROYAL GUATEMALA
Manufacturer StreetKM 20.5 CARRETERA A VILLA CANALES
Manufacturer CityVILLA CANALES
Manufacturer CountryGT
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDEROYAL
Generic NameMHW - DRESSING, COMPRESSION
Product CodeMHW
Date Received2013-07-18
Catalog NumberA131067
Lot Number28366768
OperatorLAY USER/PATIENT
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDEROYAL GUATEMALA
Manufacturer AddressGT


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2013-07-18

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