SKYN ORIGINAL NON LATEX CONDOM 12CT — Class II medical device recall Z-1530-2022
Ongoing recall by Family Dollar Stores, Llc., reported 2022-08-24, distributed nationwide. Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10
| Recall number | Z-1530-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Family Dollar Stores, Llc., Chesapeake, VA, United States |
| Recall initiated | 2022-06-23 |
| Classified | 2022-08-17 |
| Reported by FDA | 2022-08-24 |
| Distributed | Nationwide (US) |
| Quantity | 2,877 total |
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 for recall
Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1530-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.