FDA Device recall Z-0751-2019
U by Kotex¿ Sleek¿, Regular Tampons, 3 Count
- FDA Device
- Class II
- terminated
- Published 2019-01-23
On 2019-01-23 the FDA classified a Class II recall of U by Kotex¿ Sleek¿, Regular Tampons, 3 Count by Kimberly Clark, citing potential for tampon to come apart upon removal.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0751-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-12-11 |
| Published | 2019-01-23 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Kimberly Clark |
| Distribution | US |
Product
U by Kotex¿ Sleek¿, Regular Tampons, 3 Count
Reason
Potential for tampon to come apart upon removal.
Identifiers
| upc | 10036000459296 |
|---|---|
| code_info | Package UPC: 36000423372; Case UPC: 10036000459296; Lot Numbers: XM700604X, XM700904X, XM702304X, XM702404X, XM702504X. |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0751-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.