FDA Device Intelligence
HomeDevice types › MMS

Lubricant, Vaginal, Patient

FDA product code MMS · Class 1 · General Hospital

8
Registered devices
12
Adverse events
2
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2022-05-25Mckesson Medical-Surgical Inc. Corporate OfficeFacility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lot
2015-04-27Sheffield Pharmaceuticals, LLCRecovery of high count of gram positive rods including single colonies of B. cepacia.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.