Z-3024-2020 Class II Ongoing

Recalled by Office Depot Inc — Boca Raton, FL

FDA device recall Z-3024-2020 was initiated by Office Depot Inc on July 27, 2020 and is designated Class II. Reason for recall: Test results revealed that the KN95 masks failed to filter greater than 95% of particulates. The recall status is ongoing. Affected quantity: 25,360 masks.

Recall Details

Product Type
Devices
Report Date
October 7, 2020
Initiation Date
July 27, 2020
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
25,360 masks

Product Description

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.

Distribution Pattern

nationwide

Code Information

SKU 4555098 & 8510447