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 |