FDA Device recall Z-0875-2013
KY TINGLING JELLY Personal Lubricant
- FDA Device
- Class II
- terminated
- Published 2013-03-06
On 2013-03-06 the FDA classified a Class II recall of KY TINGLING JELLY 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-0875-2013 |
| 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 TINGLING JELLY Personal Lubricant. The product is packaged into 5 oz tubes with the UPC printed on it. Distributed By: McNeil-PPC Inc.
Reason
This product is not cleared for marketing in the US.
Identifiers
| upc | 380040088887 |
|---|---|
| code_info | Tube UPC: 380040088887 Case Code(s): 008888 V21, 008888 V00 Outer Case UPC: 103800400888840215, 103800400888840000 |
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-0875-2013%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.