EAR WAX REMOVER *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1998-11-19 for EAR WAX REMOVER * manufactured by Deer Creek Products.

Event Text Entries

[17480565] Potentially unsafe product in advertisement.
Patient Sequence No: 1, Text Type: D, B5

MAUDE Entry Details

• Report Number: MW1014997
• MDR Report Key: 197979
• Date Received: 1998-11-19
• Date of Report: 1998-11-04
• Date Added to Maude: 1998-11-23
• Event Key: 0
• Report Source Code: Voluntary report
• Manufacturer Link: N
• Number of Patients in Event: 0
• Adverse Event Flag: 3
• Product Problem Flag: 3
• Reprocessed and Reused Flag: 0
• Reporter Occupation: AUDIOLOGIST
• Health Professional: 3
• Initial Report to FDA: 0
• Report to FDA: 0
• Event Location: 3
• Single Use: 0
• Previous Use Code: 0
• Event Type: 3
• Type of Report: 3

Device Details

• Brand Name: EAR WAX REMOVER
• Generic Name: WAR WAX REMOVER
• Product Code: JZE
• Date Received: 1998-11-19
• Model Number: *
• Catalog Number: *
• Lot Number: *
• ID Number: *
• Operator: LAY USER/PATIENT
• Device Availability: Y
• Implant Flag: N
• Date Removed: *
• Device Sequence No: 1
• Device Event Key: 192334
• Manufacturer: DEER CREEK PRODUCTS
• Manufacturer Address: 3038 NW 25TH AVE POMPANO BEACH FL 33069 US

Patients

Patient Number	Treatment	Outcome	Date
1	0		1998-11-19