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
DFI Co. Recalls
7 recalls found for DFI Co.. Check if any of your products are affected.
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