Z-0873-2013Class II

KY SENSITIVE TM JELLY Personal Lubricant. The product is packaged into 3 oz tubes, which are then packed into...

Name: Z-0873-2013 KY SENSITIVE TM JELLY Personal Lubricant. The product is packaged into 3 oz tubes, which are then packed into...
Creator: Mc-NEIL-PPC, Inc.
Published: 2013-01-25
License: https://open.fda.gov/license/

Kenvue Brands LLC / initiated 2013-01-25 / Terminated

FDA source

Mc-NEIL-PPC, Inc. began a recall of 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 on 2013-01-25. FDA classified it as Class II and gives the reason as "This product is not cleared for marketing in the US". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0873-2013
Classification: Class II
Status: Terminated
Initiated: 2013-01-25
Posted: 2013-02-22
Terminated: 2014-04-11
Recalling firm: Kenvue Brands LLC
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.
Product code: NUC Lubricant, Personal
Reason for recall: This product is not cleared for marketing in the US.
FDA root cause: No Marketing Application
Action: Johnson and Johnson Healthcare Products sent recall notification letters dated 1/25/2013 to its customers (retailers and wholesalers). The letter identified the product, problem, and actions to be taken by the customers. Customers were asked to return all cases of affected product in their possession. The letter included delivery confirmation and a return packing slip, return authorization label and business reply card. Contact J & J Sales & Logistics at 866-912-8414 for questions regarding the return of affected product. Contact your J & J Sales & Logistics Company Sales Representative for questions about the product.
Quantity in commerce: 1,185,664 units
Distribution: Nationwide Distribution.
Product codes and lots: 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

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0873-2013
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0873-2013	Class II	Terminated	Voluntary: Firm initiated	2013-03-06	2013-02-22
Z-0874-2013	Class II	Terminated	Voluntary: Firm initiated	2013-03-06	2013-02-22
Z-0875-2013	Class II	Terminated	Voluntary: Firm initiated	2013-03-06	2013-02-22

Product code NUC

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)