FDA Device recall Z-0874-2013
KY SilkE Vaginal Moisturizer and Personal Lubricant
- FDA Device
- Class II
- terminated
- Published 2013-03-06
On 2013-03-06 the FDA classified a Class II recall of KY SilkE Vaginal Moisturizer and Personal Lubricant by Mc Neil Ppc, citing this product is not cleared for marketing in the US.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0874-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-01-25 |
| Published | 2013-03-06 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Mc Neil Ppc |
| Distribution | US |
Product
KY SilkE Vaginal Moisturizer and Personal Lubricant. The product is packaged in 2.5 oz bottles, which are then packed into a printed carton. Distributed by McNeil-PPC Inc.
Reason
This product is not cleared for marketing in the US.
Identifiers
| upc | 00380041153300 |
|---|---|
| code_info | Carton: 380040087149 Case Code: 008714 V05 Outer case UPC Code: 103800400871460055 Outer case Display UPC Code: 00380041153300 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0874-2013%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.