KY LIQUIBEADS Vaginal Moisturizer — Class II medical device recall Z-2467-2012
Terminated recall by Mc-NEIL-PPC, Inc., reported 2012-10-03, distributed nationwide. Johnson & Johnson Healthcare Products (JJHP) is voluntarily recalling this product to address FDA concerns tha
| Recall number | Z-2467-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mc-NEIL-PPC, Inc., Skillman, NJ, United States |
| Recall initiated | 2012-07-02 |
| Classified | 2012-09-27 |
| Reported by FDA | 2012-10-03 |
| Terminated | 2013-09-27 |
| Distributed | Nationwide (US) |
| Quantity | 818,712 |
| UPC / GTIN / UDI-DI | 00380040087958, 00380041087704 |
Product
KY LIQUIBEADS Vaginal Moisturizer; Distributed By: McNeil-PPC, Inc. Skillman, NJ 08558-9418; UPC 380041087704; 380040087958. Personal lubricant
Reason for recall
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2467-2012. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.