--- title: "DFI Co., Ltd. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search DFI Co., Ltd. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/dfi-co-ltd/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # DFI Co., Ltd. recall records **7** reported ongoing 7 records in this archive. Latest source date Apr 2, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Apr 2, 2026 FDA device enforcement ### [One Step 10A in vitro diagnostic test](https://isitonrecall.com/recall/fda-device-z-2082-2026-one-step-10a-in-vitro-diagnostic-test/) The devices were distributed without required FDA premarket clearance or approval. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of FL, PA and the country of England. [Official source for One Step 10A in vitro diagnostic test](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2082-2026%22) Apr 2, 2026 FDA device enforcement ### [One Step UTI in vitro diagnostic test REF: 3374](https://isitonrecall.com/recall/fda-device-z-2083-2026-one-step-uti-in-vitro-diagnostic-test-ref-3374/) The devices were distributed without required FDA premarket clearance or approval. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of FL, PA and the country of England. [Official source for One Step UTI in vitro diagnostic test REF: 3374](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2083-2026%22) Apr 2, 2026 FDA device enforcement ### [One Step pH in vitro diagnostic test REF: 31I4P](https://isitonrecall.com/recall/fda-device-z-2084-2026-one-step-ph-in-vitro-diagnostic-test-ref-31i4p/) The devices were distributed without required FDA premarket clearance or approval. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of FL, PA and the country of England. [Official source for One Step pH in vitro diagnostic test REF: 31I4P](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2084-2026%22) Apr 2, 2026 FDA device enforcement ### [QUCARE Total Cholesterol in vitro diagnostic test REF: 6407](https://isitonrecall.com/recall/fda-device-z-2085-2026-qucare-total-cholesterol-in-vitro-diagnostic-test-ref-6407/) The devices were distributed without required FDA premarket clearance or approval. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of FL, PA and the country of England. [Official source for QUCARE Total Cholesterol in vitro diagnostic test REF: 6407](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2085-2026%22) Apr 2, 2026 FDA device enforcement ### [Uric Acid in vitro diagnostic test REF: 31H0P](https://isitonrecall.com/recall/fda-device-z-2086-2026-uric-acid-in-vitro-diagnostic-test-ref-31h0p/) The devices were distributed without required FDA premarket clearance or approval. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of FL, PA and the country of England. [Official source for Uric Acid in vitro diagnostic test REF: 31H0P](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2086-2026%22) Apr 2, 2026 FDA device enforcement ### [One Step K in vitro diagnostic test REF: 81A4](https://isitonrecall.com/recall/fda-device-z-2087-2026-one-step-k-in-vitro-diagnostic-test-ref-81a4/) The devices were distributed without required FDA premarket clearance or approval. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of FL, PA and the country of England. [Official source for One Step K in vitro diagnostic test REF: 81A4](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2087-2026%22) Apr 2, 2026 FDA device enforcement ### [One Step P in vitro diagnostic test REF: 8194](https://isitonrecall.com/recall/fda-device-z-2088-2026-one-step-p-in-vitro-diagnostic-test-ref-8194/) The devices were distributed without required FDA premarket clearance or approval. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of FL, PA and the country of England. [Official source for One Step P in vitro diagnostic test REF: 8194](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2088-2026%22) ## Reasons in these listed records - The devices were distributed without required FDA premarket clearance or approval. These examples come from this result page and are not a ranking of every recall reason. ## Checking DFI Co., Ltd. ### Is there a recall on dfi co., ltd. right now? This archive contains 7 records, including 7 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search DFI Co., Ltd.](https://isitonrecall.com/check/?q=DFI%20Co.%2C%20Ltd.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)