Facility

FRIDABABY, LLC

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3030726486
Establishment type	Repack or Relabel Medical Device
Location	11007 Development Way Jacksonville, FL, US 32220
Registration status	Active · expires 2026
Parent company	Fridababy, LLC (owner-operator 10052488)
Brand names	Frida Fertility At-Home Insemination Set

Activity by year

Recalls (1)

Devices registered here (1)

Applicator, Vaginal
Product code HGD (opens in a new tab) · Class I · Obstetrics/Gynecology · 21 CFR 884.4520

Recalls & enforcement

Class IIOngoing2020-01-27
FridaBaby has been made aware through customer reports that the product is being used outside of the labeled directions. Specifically, repeated chewing or biting on the SmileFrida, the ToothHugger has caused deterioration in the outer layer of the brush and in very rare occasion…

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. “FRIDABABY, LLC (FEI 3030726486) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3030726486-fridababy-llc/

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