JINYINSHAN — Class II medical device recall Z-3024-2020
Ongoing recall by Office Depot Inc, reported 2020-10-07, distributed nationwide. Test results revealed that the KN95 masks failed to filter greater than 95% of particulates.
| Recall number | Z-3024-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Office Depot Inc, Boca Raton, FL, United States |
| Recall initiated | 2020-07-27 |
| Classified | 2020-09-28 |
| Reported by FDA | 2020-10-07 |
| Distributed | Nationwide (US) |
| Quantity | 25,360 masks |
| Reason classes | specification failure |
Product
JINYINSHAN, KN95 PROTECTIVE MASK P1, 20 pieces
Reason for recall
Test results revealed that the KN95 masks failed to filter greater than 95% of particulates.
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-3024-2020. 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.