Tampon Innovations
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
- Inspections (1)
- Warning letters (1)
Devices registered here (1)
- Applicator, Absorbent Tipped, Non-SterileProduct code KXF (opens in a new tab) · Class I · General Hospital · 21 CFR 880.6025
Recalls & enforcement
- Class IIOngoing2025-02-17Product lacks 510(k) clearance.
FDA inspections (1)
- OAI2024-07-11Official Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
FDA warning letters (1)
- Warning Letter2024-12-17Warning Letter (opens in a new tab) · Iliyantsi
Source: U.S. FDA Compliance Actions Dashboard (opens in a new tab) (device warning letters, 2016–present). Data as of 2026-10-06. Each link opens an FDA search for the letter; FDA can take several weeks to post a letter, so a very recent one may not appear yet.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Tampon Innovations (FEI 3028725772) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3028725772-tampon-innovations/
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