ABDOMINAL BINDER * A131067

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2013-07-16 for ABDOMINAL BINDER * A131067 manufactured by Deroyal Industries Inc..

Event Text Entries

[3652401] Patient developed red, non-raised, rash from abdominal binder that was used post c-section. I spoke with the clinical leader of mother baby unit and labor and delivery and they both stated there has been nothing different in either products or procedures to which they can attribute this type of event (binders causing a rash). There has been no change in l&d to the skin prep, dressings, or the or packs. The abdominal binders are placed on dry skin in labor and delivery. This facility has had more than 10 similar events with this product in the last 5 months. Product states latex free. The facility reports this type of reaction has been seen in patients with c-sections as well as vaginal deliveries; thus, staff does not believe that there is a reaction to the skin prep used for c-section deliveries because the prep is not used in a vaginal delivery. Also, staff has stated in previous incidents that the rash occurs on areas which does not have the skin prep but does have contact with the binder. Patients with and without known allergies have been affected. The manufacturer has been notified. They are unaware of any other complaints like this. We checked with our surgical unit because they use quite a few abdominal binders and they have not heard of any concerns regarding rash. Patients in the surgical unit would have similar use of this device. Also, there are patients in the surgical unit both who have and who have not had exposure to the same brand of skin prep as the patients on the other nursing unit. The storage procedure/process for both nursing units is identical: storage and transportation of the devices are not believed to be contributing factors in these events. ======================manufacturer response for abdominal binder medium/large, (brand not provided) (per site reporter). ======================i spoke with the manufacturer's rep and they stated they would send packaging label via email to return for investigation. I reminded them that i still had not received packaging labels for the three other abdominal binders i called about last week. They plan to send a label so i can return all four binders. What was the original intended procedure? Abdominal incisional support post c-section. Device #1is this a laboratory device or laboratory test? No.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3231125
MDR Report Key3231125
Date Received2013-07-16
Date of Report2013-07-16
Date of Event2013-07-11
Report Date2013-07-16
Date Reported to FDA2013-07-16
Date Reported to Mfgr2013-07-17
Date Added to Maude2013-07-17
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 NameBINDER, ABDOMINAL
Product CodeFSD
Date Received2013-07-16
Model Number*
Catalog NumberA131067
Lot Number31048058
ID Number*
OperatorPATIENT
Device AvailabilityY
Device Age*
Device Sequence No1
Device Event Key0
ManufacturerDEROYAL INDUSTRIES INC.
Manufacturer Address200 DEBUSK LANE POWELL TN 37849 US 37849


Patients

Patient NumberTreatmentOutcomeDate
10 2013-07-16

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