FDA Device recall Z-1356-2021
At Home Semi-Flex/Rigid Insemination Device (SKU 644042787903)
- FDA Device
- Class II
- ongoing
- Published 2021-04-14
On 2021-04-14 the FDA classified a Class II recall of At Home Semi-Flex/Rigid Insemination Device (SKU 644042787903) by Tenderneeds Fertility, citing device was distributed without a proper marketing authorization.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1356-2021 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2020-12-23 |
| Published | 2021-04-14 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Tenderneeds Fertility |
| Distribution | n/a |
Product
At Home Semi-Flex/Rigid Insemination Device (SKU 644042787903)
Reason
Device was distributed without a proper marketing authorization.
Identifiers
| code_info | All lots |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1356-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.