HIGH
FDA DEVICE
One Step 10A in vitro diagnostic test
The devices were distributed without required FDA premarket clearance or approval.
DFI Co.
The devices
Brand hub
DFI Co. Recalls
7 recalls found for DFI Co.. Check current safety alerts and related brands before using affected products.
- Active recalls
- 7
- Pages
- 1
HIGH
FDA DEVICE
Uric Acid in vitro diagnostic test REF: 31H0P
The devices were distributed without required FDA premarket clearance or approval.
DFI Co.
The devices
HIGH
FDA DEVICE
One Step P in vitro diagnostic test REF: 8194
The devices were distributed without required FDA premarket clearance or approval.
DFI Co.
The devices
HIGH
FDA DEVICE
One Step pH in vitro diagnostic test REF: 31I4P
The devices were distributed without required FDA premarket clearance or approval.
DFI Co.
The devices
HIGH
FDA DEVICE
One Step K in vitro diagnostic test REF: 81A4
The devices were distributed without required FDA premarket clearance or approval.
DFI Co.
The devices
HIGH
FDA DEVICE
QUCARE Total Cholesterol in vitro diagnostic test REF: 6407
The devices were distributed without required FDA premarket clearance or approval.
DFI Co.
The devices
HIGH
FDA DEVICE
One Step UTI in vitro diagnostic test REF: 3374
The devices were distributed without required FDA premarket clearance or approval.
DFI Co.
The devices
Brand Statistics
Total Recalls
7
Pages
1
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