FDA Device recall Z-0873-2013
KY SENSITIVE TM 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 SENSITIVE TM 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-0873-2013 |
| 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 SENSITIVE TM JELLY Personal Lubricant. The product is packaged into 3 oz tubes, 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 | 380040085503 |
|---|---|
| upc | 00380041153300 |
| code_info | Tube UPC: 380040085503 Case Code(s): 008550 V21, 008550 V00 Outer case UPC Code: 103800400855000215 Outer case UPC…Tube UPC: 380040085503 Case Code(s): 008550 V21, 008550 V00 Outer case UPC Code: 103800400855000215 Outer case UPC Code: 103800400855000000 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-0873-2013%22
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