FDA Device recall Z-0748-2019
U by Kotex¿ Sleek¿, Regular Tampons, 18 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, 18 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-0748-2019 |
| 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, 18 Count
Reason
Potential for tampon to come apart upon removal.
Identifiers
| upc | 10036000294535 |
|---|---|
| code_info | Package UPC: 36000294538; Case UPC: 10036000294535; Lot Numbers: NN628201B, NN726913B, NN628301A, NN728713C, NN62…Package UPC: 36000294538; Case UPC: 10036000294535; Lot Numbers: NN628201B, NN726913B, NN628301A, NN728713C, NN628301B, NN728713D, NN629101A, NN729813A, NN629101B, NN731113A, NN629201A, NN732513B, NN630201A, NN733713D, NN630201B, NN733813A, NN630301A, NN800413B, NN632713A, NN800513C, NN632713B, NN802913B, NN634713B, NN803013A, NN634813A, NN804413A, NN635713A, NN804413B, NN635713B, NN807613D, NN701813A, NN807713C, NN701813B, NN808413C, NN701913A, NN808413D, NN703213B, NN812013A, NN705713C, NN812013B, NN705713D, NN812713B, NN705813A, NN812813A, NN707613D, NN814013D, NN707713C, NN814113A, NN711513A, NN814113B, NN711513B, NN815513A, NN715213B, NN815513B, NN715313C, NN819613D, NN715313D, NN819713A, NN716713C, NN821313A, NN716713D, NN822613B, NN718313C, NN822713A, NN720713B, NN824513D, NN723413B, NN824613A, NN723513A, NN824613B, NN724913B, NN826513D, NN725013A, NN826613C, NN726913A, NN827913C. |
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-0748-2019%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.