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Medical Device

Uric Acid in vitro diagnostic test REF: 31H0P

Recall date: 2026-05-13 · Source: FDA_DEVICE
Brand / Firm
DFI Co., Ltd.
Product
Uric Acid in vitro diagnostic test REF: 31H0P
Reason for recall
The devices were distributed without required FDA premarket clearance or approval.
Units affected
59815 units
Description
Uric Acid in vitro diagnostic test REF: 31H0P
View official recall notice →