FDA Device recall Z-1530-2022
SKYN ORIGINAL NON LATEX CONDOM 12CT, SKU 903409 LS SKYN NON LATEX LUBRICATED CONDOM 3CT, SKU 900794 SKYN ELITE NON LATEX CONDOM 12CT, SKU 9…
- FDA Device
- Class II
- ongoing
- Published 2022-08-24
On 2022-08-24 the FDA classified a Class II recall of SKYN ORIGINAL NON LATEX CONDOM 12CT, SKU 903409 LS SKYN NON LATEX LUBRICATED CONDOM 3CT, SKU 900794 SKYN ELITE NON LATEX CONDOM 12CT, SKU 9… by Family Dollar Stores, citing affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1530-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-06-23 |
| Published | 2022-08-24 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Family Dollar Stores |
| Distribution | US |
Product
SKYN ORIGINAL NON LATEX CONDOM 12CT, SKU 903409 LS SKYN NON LATEX LUBRICATED CONDOM 3CT, SKU 900794 SKYN ELITE NON LATEX CONDOM 12CT, SKU 903415
Reason
Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
Identifiers
| code_info | All product sold between May 1, 2022 - June 10, 2022. |
|---|
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-1530-2022%22
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