FDA Device recall Z-3024-2020
JINYINSHAN, KN95 PROTECTIVE MASK P1, 20 pieces
- FDA Device
- Class II
- ongoing
- Published 2020-10-07
On 2020-10-07 the FDA classified a Class II recall of JINYINSHAN, KN95 PROTECTIVE MASK P1, 20 pieces by Office Depot, citing test results revealed that the KN95 masks failed to filter greater than 95% of particulates.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3024-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2020-07-27 |
| Published | 2020-10-07 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Office Depot |
| Distribution | US |
Product
JINYINSHAN, KN95 PROTECTIVE MASK P1, 20 pieces
Reason
Test results revealed that the KN95 masks failed to filter greater than 95% of particulates.
Identifiers
| code_info | SKU 4555098 & 8510447 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3024-2020%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.