Recall
FDAHealthApril 2, 2026

DFI Co., Ltd. — One Step pH in vitro diagnostic test REF: 31I4P

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

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
April 2, 2026

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

What's affected?

Product
One Step pH in vitro diagnostic test REF: 31I4P
Lot code
250305

Additional details

UDI: 08806141303060/ Lot: 250305, 250415, 250509, 250625, 250905

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 7860 units.

View original FDA notice →

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