FDA Medical Device Recalls (openFDA)
Office Depot Inc: JINYINSHAN, KN95 PROTECTIVE MASK P1, 20 pieces
- Recall number
- Z-3024-2020
- Recalling firm
- Office Depot Inc
- Product
- JINYINSHAN, KN95 PROTECTIVE MASK P1, 20 pieces
- Status
- Open, Classified
- Initiated
- 2020-07-27
- Posted
- not on file
- Terminated
- not on file
- Reason
- Test results revealed that the KN95 masks failed to filter greater than 95% of particulates.
- Root cause
- Other
- Action
- The firm notified its consignees be email on 07/29/2020. The notice indicated that the product was tested and did not live up to expectations. The firm is offering a replacement of the product.
- Quantity
- 25,360 masks
- Distribution
- nationwide
- Lot, serial or model codes
- SKU 4555098 & 8510447
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- NZJ
- Firm FEI
- 3000122585
- Firm city
- Boca Raton
- Firm state
- FL
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28