MEDICHOICE *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-02-12 for MEDICHOICE * manufactured by Owens & Minor.

Event Text Entries

[5482570] Patient developed rash with itching where abdominal binder was located.
Patient Sequence No: 1, Text Type: D, B5

MAUDE Entry Details

• Report Number: 4588948
• MDR Report Key: 4588948
• Date Received: 2015-02-12
• Date of Report: 2015-02-12
• Date of Event: 2015-01-11
• Report Date: 2015-02-12
• Date Reported to FDA: 2015-02-12
• Date Reported to Mfgr: 2015-03-11
• Date Added to Maude: 2015-03-11
• Event Key: 0
• Report Source Code: User Facility report
• Manufacturer Link: N
• Number of Patients in Event: 0
• Adverse Event Flag: 3
• Product Problem Flag: 3
• Reprocessed and Reused Flag: 0
• Health Professional: 3
• Initial Report to FDA: 3
• Report to FDA: 3
• Event Location: 3
• Single Use: 0
• Previous Use Code: 0
• Event Type: 3
• Type of Report: 3

Device Details

• Brand Name: MEDICHOICE
• Generic Name: ABDOMINAL BINDER
• Product Code: FSD
• Date Received: 2015-02-12
• Model Number: *
• Catalog Number: *
• Lot Number: *
• ID Number: *
• Operator: PATIENT
• Device Availability: Y
• Device Sequence No: 1
• Device Event Key: 0
• Manufacturer: OWENS & MINOR
• Manufacturer Address: 9120 LOCKWOOD BLVD MECHANICSVILLE VA 23116 US 23116

Patients

Patient Number	Treatment	Outcome	Date
1	0		2015-02-12