FDA Device Intelligence
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Lubricant, Personal

FDA product code NUC · Class 2 · Obstetrics/Gynecology

1,601
Registered devices
171
Adverse events
7
Recalls
247
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2022-06-23Family Dollar Stores, Llc.Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
2013-01-25Mc-NEIL-PPC, Inc.This product is not cleared for marketing in the US.
2013-01-25Mc-NEIL-PPC, Inc.This product is not cleared for marketing in the US.
2013-01-25Mc-NEIL-PPC, Inc.This product is not cleared for marketing in the US.
2012-07-02Mc-NEIL-PPC, Inc.Johnson & Johnson Healthcare Products (JJHP) is voluntarily recalling this product to address FDA concerns that the product should have been cleared under a sep
2009-07-10Memphis Fertility Laboratory IncProduct was marketed without a 510(k).
2008-09-22INGfertility, LLCProduct contaminated with bacteria (Brachybacterium rhamnosum, a non pathogen gram positive cocci).

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.