Tenderneeds Fertility recalls home pregnancy and ovulation tests sold before Dec 9, 2019 due to lack of proper marketing authorization. No immediate action needed but check if you own the product.
Device was distributed without a proper marketing authorization. This event is an expansion of RES 87581, Z-1355-2021 thru Z-1364-2021.
Tenderneeds Fertility is recalling home artificial insemination kits sold before December 9, 2019 because they were distributed without proper marketing authorization. This means the product may not meet safety standards for use.
The product was distributed without proper marketing authorization, meaning it may not meet safety standards for use. This could lead to incorrect results or other issues if the product is used without proper oversight.
People who purchased the Tenderneeds Fertility Home Artificial Insemination Kit with SKU midiuikt before December 9, 2019 are likely affected. Those using the product for fertility testing may be at slightly higher risk due to unapproved marketing.
Check for the SKU midiuikt on the product label. The kit was sold before December 9, 2019. If you bought it from a retailer that sold it before that date, it's likely affected.
Look for the SKU midiuikt on the product label to confirm if it's recalled.
The recall is due to lack of proper marketing authorization, not an immediate safety hazard. No serious injury risk is mentioned.
No immediate action is required. The recall is for unapproved marketing, not a safety issue that requires stopping use.
The product was sold before December 9, 2019.
We’ve drafted a message you can send Tenderneeds Fertility to request your refund or repair — edit it as you like.
Subject: Recall Z-2176-2021 — Tenderneeds Fertility Tenderneeds Fertility Hello, I own a Tenderneeds Fertility that is covered by recall Z-2176-2021 from Tenderneeds Fertility. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
