Reported May 13, 2026 · Ongoing

QUCARE Total Cholesterol in vitro diagnostic test REF: 6407

DFI Co., Ltd.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: DFI Co., Ltd. · 388-25 Gomo-Ro · Gimhae · N/A

Is this the product you have?

  • QUCARE Total Cholesterol
  • in vitro diagnostic test REF6407
Lot codes and dates
  • UDI08806141303060/
  • Lot
    • BS032501
    • BS042502
    • BS062501
    • BS062502
    • BS082501
Amount recalled
6398 units

This recall covers 7 products

The agency filed one notice per product. You are reading one of them; the other 6 are below.

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:38 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.