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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Tenderneeds Fertility LLC: Device was distributed without a proper marketing authorization.

Agency Publication Date: April 6, 2021
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Affected Products

Product: At Home Artificial Intrauterine Insemination Kit (SKU 636391205825, 636391205894, 636391205900, 636391205924, 636391205863, 636391205931, 636391205849, 636391206020, 644042787583, 636391205917, and 636391205801)

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Product: At Home Semi-Flex/Rigid Insemination Device (SKU 644042787903)

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Product: At Home Artificial Intrauterine Insemination Flex Set (SKU 636391205870)

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Product: Deluxe At Home Pro Series Insemination Kit (SKU 644042787958)

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Product: Deluxe At Home Artificial Insemination Kit (SKU 636391205832)

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Product: Premium At Home Pro Series Insemination Kit (SKU 644042787927)

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Product: Professional Artificial Intrauterine Insemination Kit (SKU 636391205986)

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Product: Professional Clinical Artificial Intrauterine Insemination Kit (SKU 636391205962, 636391206013)

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Product: Pro Series Fertility Device (SKU 644042788139)

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Product: Professional At Home Artificial Intrauterine Insemination Set (SKU 644042787811)

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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87581
Status: Active
Manufacturer: Tenderneeds Fertility LLC
Manufactured In: United States
Units Affected: 10 products (Unknown; Unknown; Unknown; Unknown; Unknown; Unknown; Unknown; Unknown; Unknown; Unknown)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.