FDADecember 23, 2020device
At Home Semi-Flex/Rigid Insemination Device (SKU 644042787903)
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Device was distributed without a proper marketing authorization.
What to do
FDA enforcement status: Ongoing
Brands named
tenderneeds fertilitytenderneeds
UPCs
644042787903
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDA2 X Sterile Human Home Artificial Insemination Semen Kit (Human), SKU 1432985929602020-12-23
- FDATenderNeeds Fertility PRO IUI Human Artificial Home Insemination Kits, SKU 1331660557712020-12-23
- FDAAt Home Artificial Intrauterine Insemination Kit (SKU 636391205825, 636391205894, 636391205900, 636391205924, 636391205863, 636391205931, 636391205849, 636391206020, 644042787583, 636391205917, and 636391205801)2020-12-23
- FDADeluxe At Home Pro Series Insemination Kit (SKU 644042787958)2020-12-23
- FDADeluxe At Home Artificial Insemination Kit (SKU 636391205832)2020-12-23
- FDAProfessional Artificial Intrauterine Insemination Kit (SKU 636391205986)2020-12-23
- FDAProfessional Clinical Artificial Intrauterine Insemination Kit (SKU 636391205962, 636391206013)2020-12-23
- FDAUltimate Fertility At Home Insemination Kit with Sperm Wash Medium, SKU ULTFKSW2020-12-23
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