Recall events
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Event 83429
Event summary
Timeline bucket July 25, 2019
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording NeuroLogica Corporation
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
2 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 2
HS70A Diagnostic Ultrasound System Version 2.01.00, 2.01.01, 2.01.02, 2.01.03, 2.01.04, 2.01.05, 2.01.06, 1.00.06, 1.00.07, 1.00.08, 1.00.09, 1.00.10, 1.00.11, 1.00.12
Z-2275-2019
Recall number Z-2275-2019
Initiated July 25, 2019
Classification Class II
Status Terminated
Quantity 3582 worldwide
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
There is a potential for probes overheating when decreasing the Doppler SV (Sample Volume) size value set by the user in the Doppler Only mode.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2275-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27231]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a potential for probes overheating when decreasing the Doppler SV (Sample Volume) size value set by the user in the Doppler Only mode.
Code information UDI: 08806167789220 Serial Numbers: S1C0M3HK300004A S1C0M3HK300005P S1C0M3HK300006D S1C0M3HK300007X S1C0M3HK300008N S1C0M3HK300001K S1C0M3HK300002Z S1C0M3HK400005Z S1C0M3HK400006Y S1C0M3HK400008P S1C0M3HK400001L S1C0M3HK400002T S1C0M3HK400003B S15NM3HK200005N S15NM3HK100001X S1C0M3HKC00001H S1C0M3HKC00002J S1C0M3HK900001Z S1C0M3HK900002Y S1C0M3HK900003A S1C0M3HK900004P S1C0M3HK900005D S1C0M3HK900006X S1C0M3HK900007N S1C0M3HK900008E S1C0M3HK900009F S1C0M3HK900010L S1C0M3HK900011T S1C0M3HK800001P S1C0M3HK800002D S1C0M3HK700001N S1C0M3HK700002E
Distribution pattern US Nationwide
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[29171]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 2
WS80A Diagnostic Ultrasound System Version 1.00.16, 3.00.17, 3.00.18, 3.00.19, 3.01.00, 3.01.01, 3.01.02, 3.01.03, 3.01.04, 3.01.05, 3.01.06, 3.01.07, 3.01.08, 3.01.09, 4.00.08, 4.00.09, 4.00.10, 4.00.11, 4.01.00, 4.01.01, 4.01.02, 4.01.03, 4.01.04, 4.01.05, 4.01.06, 4.01.07, 4.01.08, 4.01.09.
Z-2276-2019
Recall number Z-2276-2019
Initiated July 25, 2019
Classification Class II
Status Terminated
Quantity 5088 worldwide
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
There is a potential for probes overheating when decreasing the Doppler SV (Sample Volume) size value set by the user in the Doppler Only mode.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2276-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44601]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall There is a potential for probes overheating when decreasing the Doppler SV (Sample Volume) size value set by the user in the Doppler Only mode.
Code information UDI: 08806167780081 Serial Numbers: S116M3HJ600006V S116M3HJ600002H S116M3HJ400012W S116M3HJ400013V S18EM3HJA00002B S18EM3HK900002Y S18EM3HK800001P S18EM3HJB00003L S18EM3HJB00004T S18EM3HJB00005B S116M3HJ600008T S116M3HJ500005T S18EM3HJB00001W S18EM3HJB00002V S18EM3HJB00006K S18EM3HJA00003K S18EM3HJ900017P S18EM3HJ900018D S18EM3HK800005E S18EM3HK700012D S1B1M3HK100001X S18EM3HK700011P S18EM3HK700013X S18EM3HK700007M S18EM3HK700009V S18EM3HK700010A S18EM3HK700005H S18EM3HK700006J S18EM3HK700001N S18EM3HK700003F S18EM3HK700004R S18EM3HK900001Z S18EM3HK900003A S18EM3HK900005D S18EM3HK700008W S18EM3HK800002D S18EM3HK800003X S18EM3HK800004N S116M3HJ500004L S18EM3HJA00001T S18EM3HK900006X S18EM3HK900007N S18EM3HK900008E S18EM3HK900009F S18EM3HK900010L S18EM3HKC00001H S18EM3HKC00002J S18EM3HK900004P S18EM3HK800006F S18EM3HK700002E S18EM3HM500009Y S18EM3HM500010F S18EM3HM500011R S18EM3HM500012H S18EM3HM500007K S18EM3HM500008Z S18EM3HM500001M S18EM3HM500002W S18EM3HM500003V S18EM3HM500004L S18EM3HM500005T S18EM3HM500006B S18EM3HM400001L
Distribution pattern US Nationwide
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[28939]
FDA event record
· Exact recall-number query on openFDA