FDA Adverse Event Malfunction Summary report: N

U BY KOTEX CLICK : TAMPON, MENSTRUAL, UNSCENTED : HEB

MDR report key: 11983171 · Received June 11, 2021

Report

Report Number
3011109575-2021-00206
Event Type
Malfunction
Date Received
June 11, 2021
Date of Event
May 12, 2021
Report Date
June 11, 2021
Manufacturer
K-C AFC MANUFACTURING, S. DE R.L. DE C.V
Product Code
HEB
UDI-DI
00036000515893
PMA / PMN Number
K172118
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 1

REVIEW OF THE DEVICE HISTORY RECORD (DHR) AND SUPPORTING QUALITY RECORDS CONFIRMED NO ANOMALIES THAT MAY HAVE CAUSED OR CONTRIBUTED TO THE MALFUNCTION.

Description of Event or Problem · 1

CONSUMER REPORTED THE TAMPONS FELL APART LEAVING PIECES INSIDE HER VAGINAL CAVITY. SHE DEVELOPED YEAST INFECTION LIKE SYMPTOMS WITH ITCHINESS AND SWELLING OF THE VAGINAL AREA. SHE SELF-TREATED WITH A VINEGAR DOUCHE AND AZO. HER SYMPTOMS WERE NOT IMPROVING SO SHE CALLED AND SPOKE WITH HER HEALTHCARE PROVIDER. THEY PRESCRIBED BORIC ACID SUPPOSITORIES AND HER SYMPTOMS IMPROVED. SHE DID NOT SEEK ANY ADDITIONAL MEDICAL ATTENTION AND DID NOT EXPERIENCE ANY ADVERSE HEALTH EFFECTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
882050 U BY KOTEX CLICK : TAMPON, MENSTRUAL, UNSCENTED : HEB TAMPON, MENSTRUAL, UNSCENTED HEB K-C AFC MANUFACTURING, S. DE R.L. DE C.V SUPER NN105713C0740 00036000515893

Patients

Seq Age Sex Outcome Treatment
1 36 YR