Z-1358-2021Class II

Deluxe At Home Pro Series Insemination Kit (SKU 644042787958)

Name: Z-1358-2021 Deluxe At Home Pro Series Insemination Kit (SKU 644042787958)
Creator: Tenderneeds Fertility LLC
Published: 2020-12-23
License: https://open.fda.gov/license/

Tenderneeds Fertility LLC / initiated 2020-12-23 / Open, Classified

FDA source

Tenderneeds Fertility LLC began a recall of Deluxe At Home Pro Series Insemination Kit (SKU 644042787958) on 2020-12-23. FDA classified it as Class II and gives the reason as "Device was distributed without a proper marketing authorization". As of 2026-09-10, the recall status on record is Open, Classified.

Recall record

Recall number: Z-1358-2021
Classification: Class II
Status: Open, Classified
Initiated: 2020-12-23
Posted: 2021-04-06
Recalling firm: Tenderneeds Fertility LLC
Product: Deluxe At Home Pro Series Insemination Kit (SKU 644042787958)
Product code: MQF Catheter, Assisted Reproduction
Reason for recall: Device was distributed without a proper marketing authorization.
FDA root cause: No Marketing Application
Action: On December 23, 2020, the firm published a recall notification on its website at the following URL: https://tenderneedsfertility.com/recalls The notification notified customers that all IUI and ICI kits sold for human use were being recalled. Customers were instructed to destroy these products, including leftover portions, immediately. The firm did not ask customers to return the product.
Quantity in commerce: Unknown
Distribution: World-wide distribution.
Product codes and lots: All lots

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1358-2021
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1355-2021	Class II	Ongoing	Voluntary: Firm initiated	2021-04-14	2021-04-06
Z-1356-2021	Class II	Ongoing	Voluntary: Firm initiated	2021-04-14	2021-04-06
Z-1357-2021	Class II	Ongoing	Voluntary: Firm initiated	2021-04-14	2021-04-06
Z-1358-2021	Class II	Ongoing	Voluntary: Firm initiated	2021-04-14	2021-04-06
Z-1359-2021	Class II	Ongoing	Voluntary: Firm initiated	2021-04-14	2021-04-06
Z-1360-2021	Class II	Ongoing	Voluntary: Firm initiated	2021-04-14	2021-04-06
Z-1361-2021	Class II	Ongoing	Voluntary: Firm initiated	2021-04-14	2021-04-06
Z-1362-2021	Class II	Ongoing	Voluntary: Firm initiated	2021-04-14	2021-04-06
Z-1363-2021	Class II	Ongoing	Voluntary: Firm initiated	2021-04-14	2021-04-06
Z-1364-2021	Class II	Ongoing	Voluntary: Firm initiated	2021-04-14	2021-04-06

Product code MQF

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)