Recall events
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Event 98739
Event summary
Timeline bucket April 02, 2026
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording DFI Co., Ltd.
Dossier provenance
Source snapshots represented here
openFDA Device Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall
event_date_initiated coverage
June 01, 1997–June 30, 2026
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Complete imported group
Every recalled product in this event
7 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
device · product 1 of 7
One Step 10A in vitro diagnostic test
Z-2082-2026
Recall number Z-2082-2026
Initiated April 02, 2026
Classification Class II
Status Ongoing
Quantity 6533 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The devices were distributed without required FDA premarket clearance or approval.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2082-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[56166]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The devices were distributed without required FDA premarket clearance or approval.
Code information UDI: 08806141303497/ Lot: 241023, 250305, 250415, 250527, 250625, 250905
Distribution pattern Worldwide - US Nationwide distribution in the states of FL, PA and the country of England.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[543]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 7
One Step UTI in vitro diagnostic test REF: 3374
Z-2083-2026
Recall number Z-2083-2026
Initiated April 02, 2026
Classification Class II
Status Ongoing
Quantity 2423 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The devices were distributed without required FDA premarket clearance or approval.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2083-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11790]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The devices were distributed without required FDA premarket clearance or approval.
Code information UDI: 08806141303480/ Lot: 241023, 250625, 250905
Distribution pattern Worldwide - US Nationwide distribution in the states of FL, PA and the country of England.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[533]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 7
One Step pH in vitro diagnostic test REF: 31I4P
Z-2084-2026
Recall number Z-2084-2026
Initiated April 02, 2026
Classification Class II
Status Ongoing
Quantity 7860 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The devices were distributed without required FDA premarket clearance or approval.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2084-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[46809]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The devices were distributed without required FDA premarket clearance or approval.
Code information UDI: 08806141303060/ Lot: 250305, 250415, 250509, 250625, 250905
Distribution pattern Worldwide - US Nationwide distribution in the states of FL, PA and the country of England.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[531]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 7
QUCARE Total Cholesterol in vitro diagnostic test REF: 6407
Z-2085-2026
Recall number Z-2085-2026
Initiated April 02, 2026
Classification Class II
Status Ongoing
Quantity 6398 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The devices were distributed without required FDA premarket clearance or approval.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2085-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32755]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The devices were distributed without required FDA premarket clearance or approval.
Code information UDI: 08806141303060/ Lot: BS032501, BS042502, BS062501, BS062502, BS082501
Distribution pattern Worldwide - US Nationwide distribution in the states of FL, PA and the country of England.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[39269]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 7
Uric Acid in vitro diagnostic test REF: 31H0P
Z-2086-2026
Recall number Z-2086-2026
Initiated April 02, 2026
Classification Class II
Status Ongoing
Quantity 59815 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The devices were distributed without required FDA premarket clearance or approval.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2086-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32763]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The devices were distributed without required FDA premarket clearance or approval.
Code information UDI: 08806141303077/ Lot: 241023, 250415, 250509, 250617, 250905
Distribution pattern Worldwide - US Nationwide distribution in the states of FL, PA and the country of England.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[523]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 7
One Step K in vitro diagnostic test REF: 81A4
Z-2087-2026
Recall number Z-2087-2026
Initiated April 02, 2026
Classification Class II
Status Ongoing
Quantity 761 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The devices were distributed without required FDA premarket clearance or approval.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2087-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[56173]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The devices were distributed without required FDA premarket clearance or approval.
Code information UDI:08806141302650/ Lot: 241023, 250625, 250905
Distribution pattern Worldwide - US Nationwide distribution in the states of FL, PA and the country of England.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[491]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 7
One Step P in vitro diagnostic test REF: 8194
Z-2088-2026
Recall number Z-2088-2026
Initiated April 02, 2026
Classification Class II
Status Ongoing
Quantity 1064 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The devices were distributed without required FDA premarket clearance or approval.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
No Marketing Application
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2088-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5857]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall 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.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[39273]
FDA event record
· Exact recall-number query on openFDA
