Recall
Active
FDA
Official source
DFI Co., Ltd.: One Step K in vitro diagnostic test REF: 81A4 Recall
The devices were distributed without required FDA premarket clearance or approval. Product details: One Step K in vitro diagnostic test REF: 81A4
- Company
- DFI Co., Ltd.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration