Tenderneeds Fertility Recalls Professional Artificial Intrauterine Insemination Kit
Tenderneeds Fertility LLC is recalling its Professional Artificial Intrauterine Insemination Kit because it was distributed without proper marketing authorization.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically corresponds to a moderate severity level. The hazard is a regulatory compliance issue (lack of marketing authorization) rather than a direct physical defect or reported injury.
Plain-English summary
Tenderneeds Fertility LLC is recalling the Professional Artificial Intrauterine Insemination Kit (SKU 636391205986). The recall was initiated because the device was distributed without a proper marketing authorization.
The recall covers all lots of the product. The device was distributed worldwide.
Consumers who have this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- Professional Artificial Intrauterine Insemination Kit (SKU 636391205986)
- Manufacturer
- Tenderneeds Fertility LLC
- Category
- Medical Device — Fertility
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All lots
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 10 recalled by Tenderneeds Fertility LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 10 products in this recall →Related recalls
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