FDA Adverse Event Injury Summary report: N

Q-TIP

MDR report key: 2465618 · Received February 9, 2012

Report

Report Number
MW5024309
Event Type
Injury
Date Received
February 9, 2012
Date of Event
January 26, 2012
Report Date
February 9, 2012
Manufacturer
UNILEVER
Product Code
KXF
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
DE, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

THE CONSUMER SAYS THAT HE USED THE Q-TIP AND THE COTTON SEPARATED FROM THE STEM. HE WENT TO A HEARING AID SPECIALIST AND A SCOPE TEST FOUND THAT HE HAD COTTON IN HIS EAR. HE SAYS THAT IT ATTRIBUTED TO HIS HEARING PROBLEM AND THE PAIN IN HIS EAR. THE CONSUMER SAID HE CALLED THE MFR AND LEFT A MESSAGE LAST WEEK AND AGAIN TODAY. THEY HAVE YET TO RETURN HIS CALL. DOCUMENT NUMBER: (B)(4). RETAILER: RENDERS SUPERMARKET. PURCHASE DATE: (B)(6) 2012: THIS DATE IS AN ESTIMATE. THE PRODUCT WAS NOT DAMAGED BEFORE THE INCIDENT. THE PRODUCT WAS NOT MODIFIED BEFORE THE INCIDENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 Q-TIP Q-TIP KXF UNILEVER

Patients

Seq Age Sex Outcome Treatment
1