Recall Z-3024-2020— Office Depot Inc
Class II · Ongoing
Class II FDA medical device recall by Office Depot Inc, initiated 2020-07-27. FDA's recall record names no specific 510(k) clearance for this event. Product: JINYINSHAN, KN95 PROTECTIVE MASK P1, 20 pieces. Reason: Test results revealed that the KN95 masks failed to filter greater than 95% of particulates..
- Recalling firm
- Office Depot Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2020-07-27
- Firm location
- Boca Raton, FL, United States
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.