ABDOMINAL BINDER * A131056

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2014-04-04 for ABDOMINAL BINDER * A131056 manufactured by Deroyal Industries Inc.

Event Text Entries

[17951781] Patient put abdominal binder on directly to her skin last night and early in the morning. The rn was called into the room and patient had rashes where the binder was applied. This facility has had ongoing issues with this device. Multiple patients have been involved over approximately 1 year. Patients who have had c-sections and those who have had vaginal deliveries have been affected. The facility does not know why this is occurring. Patients with and without known allergies have been affected. The facility has notified the manufacturer in the past and has returned product. The problem persists.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3732939
MDR Report Key3732939
Date Received2014-04-04
Date of Report2014-04-04
Date of Event2014-02-20
Report Date2014-04-04
Date Reported to FDA2014-04-04
Date Reported to Mfgr2014-04-08
Date Added to Maude2014-04-08
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
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
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameABDOMINAL BINDER
Generic NameABDOMINAL BINDER
Product CodeFSD
Date Received2014-04-04
Model Number*
Catalog NumberA131056
Lot Number33405645
ID Number*
Device AvailabilityY
Device Age1 DAY
Device Sequence No1
Device Event Key0
ManufacturerDEROYAL INDUSTRIES INC
Manufacturer Address200 DEBUSK LANE POWELL TN 37849 US 37849


Patients

Patient NumberTreatmentOutcomeDate
10 2014-04-04

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