Devices › Tampon, menstrual, unscented
Device brand name · Tampon menstrual unscented
U By Kotex Click: medical device reports filed with FDA
600 reports name it, 2012–2023. Manufacturer given most often on reports: K-C Afc Manufacturing S De R L De C V. Product code HEB.
- 600
- device reports naming the brand
- 0% of all MAUDE reports · about 43 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 96%
- classified as malfunction
- 89.5% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
FDA's MAUDE database holds 600 reports that name the brand "U By Kotex Click" (tampon menstrual unscented), received between August 2012 and November 2023; the manufacturer given most often on reports is K-C Afc Manufacturing S De R L De C V. Spellings of one product vary from report to report.
0 reports arrived in the 12 months to August 2026, and none in the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are malfunction (96%) and injury (4%); across all tampon, menstrual, unscented reports (product code HEB) death is recorded in 0.1% and malfunction in 89.5%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are material separation (85.8%), difficult to remove (4.5%) and material fragmentation (2.5%). The patient problems coded most often are device embedded in tissue or plaque, bacterial infection and pain. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Reports by month, five years
Reports by the month FDA received them. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 11,919 reports carrying product code HEB. Event type is the filer's classification and is not verified by FDA.
Device problems coded
| Device problem (FDA code) | Reports | Share | Share across product code |
|---|---|---|---|
| Material separation | 515 | 85.8% | 46.3% |
| Difficult to removethe device was hard to remove | 27 | 4.5% | 5.3% |
| Material fragmentation | 15 | 2.5% | 2.3% |
| Breakthe device broke | 11 | 1.8% | 7.3% |
| Device operates differently than expectedthe device behaved unexpectedly | 10 | 1.7% | 0.4% |
| Material disintegration | 10 | 1.7% | 0.5% |
| Device contamination with chemical or other material | 6 | 1% | 0.2% |
| Material integrity problema problem with the device material | 6 | 1% | 0.7% |
| Detachment of device component | 5 | 0.8% | 2.4% |
| Unraveled material | 5 | 0.8% | 0.7% |
| Component missing | 3 | 0.5% | 3.3% |
| Material frayed | 3 | 0.5% | 0.1% |
| Detachment of device or device componentpart of the device came off | 2 | 0.3% | 0.2% |
| Device contamination with biological material | 2 | 0.3% | 0.1% |
| Device contamination with body fluid | 2 | 0.3% | 0.1% |
| Device damaged prior to usethe device was damaged before use | 2 | 0.3% | 0.1% |
| Device packaging compromised | 2 | 0.3% | 0% |
| Difficult to insertthe device was hard to insert | 2 | 0.3% | 0.2% |
| Insufficient device problem information | 2 | 0.3% | 16.7% |
| Stretched | 2 | 0.3% | 0.1% |
FDA's device problem codes as entered on the report; one report can carry several. Generic codes such as "no apparent adverse event" are left out.
Patient problems coded
| Patient problem (FDA code) | Reports | Share |
|---|---|---|
| Device embedded in tissue or plaque | 62 | 10.3% |
| Bacterial infectiona bacterial infection | 30 | 5% |
| Painpain, site not specified | 28 | 4.7% |
| Abdominal painstomach or belly pain | 25 | 4.2% |
| Abnormal vaginal discharge | 25 | 4.2% |
| Discomfortdiscomfort | 14 | 2.3% |
| Nauseafeeling sick | 11 | 1.8% |
| Urinary tract infectionbladder or urinary infection | 11 | 1.8% |
| Irritationirritation | 9 | 1.5% |
| Fever | 8 | 1.3% |
| Vomitingbeing sick | 8 | 1.3% |
| Abdominal cramps | 7 | 1.2% |
| Fungal infectiona fungal infection | 7 | 1.2% |
| Inflammationinflammation | 7 | 1.2% |
| Toxic shock syndrome | 6 | 1% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | U By Kotex Click | Product code HEB | All MAUDE reports |
|---|---|---|---|
| Reports | 600 | 11,919 | 26,136,888 |
| Share of that pool | — | 5% | 0% |
| Classified as death, per 1,000 reports | 0 | 1 | 9 |
| Classified as injury | 4% | 9.4% | 36.2% |
| Classified as malfunction | 96% | 89.5% | 62.3% |
| Filed by the manufacturer | 99.5% | 95.5% | 94.9% |
Shares are of reports, not of devices in use. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Other brands with product code HEB
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| U by Kotex Click : Tampon, Menstrual, Unscented : HEB | 2,373 | 57 | 0% |
| U By Kotex Sleek | 1,288 | 0 | 0% |
| U By Kotex Security Tampon Menstrual Unscented Heb | 912 | 0 | 0% |
| U By Kotex Unknown Tampon Menstrual Unscented Heb | 729 | 0 | 0% |
| Tampax Tampon, Version/Absorbency/Scent Unknown | 610 | 83 | 0% |
| U By Kotex Sleek Tampon Menstrual Unscented Heb | 504 | 0 | 0% |
| U By Kotex Click Tampons | 373 | 0 | 0% |
| U By Kotex Security | 266 | 0 | 0% |
Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA also states that "common products may have a higher number of adverse events due to the higher total number of people using the product."
Questions about U By Kotex Click reports
How many FDA reports name U By Kotex Click?
600 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 0 in the latest 12 months.
What kinds of events are reported?
malfunction (96%) and injury (4%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
material separation (85.8%), difficult to remove (4.5%), material fragmentation (2.5%), break (1.8%) and device operates differently than expected (1.7%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99.5%) and voluntary reports (0.5%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that U By Kotex Click was at fault?
No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA adds that "a causal relationship cannot be established between product and reactions listed in a report."
How do I report a problem with a medical device?
Through FDA MedWatch (Form FDA 3500 for health professionals and consumers), or to the manufacturer. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. A report counts here when any device it lists carries this brand name after punctuation and capitalisation are normalised. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.