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Recall Observatory FDA recall evidence

Device product

One Step P in vitro diagnostic test REF: 8194

Z-2088-2026

April 02, 2026

Class II

Product summary

Firm
DFI Co., Ltd.
Event
Event 98739
Status
Ongoing
Classification
Class II
Quantity
1064 units
Official record key
device-enforcement:Z-2088-2026

Official wording

Reason: The devices were distributed without required FDA premarket clearance or approval.

Code information: UDI:08806141302025/ Lot: 241023, 250527, 250905

Distribution pattern: Worldwide - US Nationwide distribution in the states of FL, PA and the country of England.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The devices were distributed without required FDA premarket clearance or approval.