FDA Device Intelligence
HomeDevice types › HEB

Tampon, Menstrual, Unscented

FDA product code HEB · Class 2 · Obstetrics/Gynecology

1,807
Registered devices
11,865
Adverse events
36
Recalls
189
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-12-26GOLD STAR DISTRIBUTION INCPotential exposure of rodents and rodent activity in the distribution center.
2025-02-17DAYE (ANNE'S DAY LTD)Product lacks 510(k) clearance.
2025-02-17DAYE (ANNE'S DAY LTD)Product lacks 510(k) clearance.
2025-02-17DAYE (ANNE'S DAY LTD)Product lacks 510(k) clearance.
2025-02-17DAYE (ANNE'S DAY LTD)Product lacks 510(k) clearance.
2025-02-17DAYE (ANNE'S DAY LTD)Product lacks 510(k) clearance.
2025-02-17DAYE (ANNE'S DAY LTD)Product lacks 510(k) clearance.
2025-02-17DAYE (ANNE'S DAY LTD)Product lacks 510(k) clearance.
2025-02-17DAYE (ANNE'S DAY LTD)Product lacks 510(k) clearance.
2025-02-17DAYE (ANNE'S DAY LTD)Product lacks 510(k) clearance.

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