RecallRadar

FDA Device recall Z-2467-2012

KY LIQUIBEADS Vaginal Moisturizer

On 2012-10-03 the FDA classified a Class II recall of KY LIQUIBEADS Vaginal Moisturizer by Mc Neil Ppc, citing johnson & Johnson Healthcare Products (JJHP) is voluntarily recalling this product to address FDA concerns that the product should have been cleared under a separate medical devic….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2467-2012
ClassificationClass II
Statusterminated
Initiated2012-07-02
Published2012-10-03
Last updated2026-09-13 11:53 UTC
CompanyMc Neil Ppc
DistributionUS

Product

KY LIQUIBEADS Vaginal Moisturizer; Distributed By: McNeil-PPC, Inc. Skillman, NJ 08558-9418; UPC 380041087704; 380040087958. Personal lubricant

Reason

Johnson & Johnson Healthcare Products (JJHP) is voluntarily recalling this product to address FDA concerns that the product should have been cleared under a separate medical device application. This voluntary recall is not being conducted on the basis of any consumer safety or product performance issues related to K-Y LIQUIBEADS. JJHP received a Warning Letter on May 23, 2012 indicating that thi

Identifiers

upc380041087704
code_info
The following Lot Numbers were identified: 2721W; 2591W; 2321W; 1681W; 0921W; 0651W; 0471W; 0361W; 0221W; 0041W; 0110H…The following Lot Numbers were identified: 2721W; 2591W; 2321W; 1681W; 0921W; 0651W; 0471W; 0361W; 0221W; 0041W; 0110H; 0100H; 0090H; 0080H; 0030H; 0179H; 0159H; 0219H and 3489RT.

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-2467-2012%22

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