Recall events
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Event 92735
Event summary
Timeline bucket July 07, 2023
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording Advance Medical Designs, Inc.
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
6 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 6
ASG-001; Ultrasound gel
Z-2532-2023
Recall number Z-2532-2023
Initiated July 07, 2023
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
mislabeled
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Other
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2532-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[33896]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
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Inspect official wording and provenance
Reason for recall Ultrasound gel mislabeled with inappropriate use.
Code information Not individually distributed
Distribution pattern US, Canada, UK, Panama, Netherlands
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[7019]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 6
50-GEL20; Ultrasound gel
Z-2533-2023
Recall number Z-2533-2023
Initiated July 07, 2023
Classification Class II
Status Ongoing
Quantity 13750 units
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
mislabeled
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Other
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2533-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[16770]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Ultrasound gel mislabeled with inappropriate use.
Code information Lot Number 21043C2328
Distribution pattern US, Canada, UK, Panama, Netherlands
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[6360]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 6
Procedural kits containing ultrasonic transmission gel, Item Numbers: a) 20-PMT03, b) 20PMT04
Z-2534-2023
Recall number Z-2534-2023
Initiated July 07, 2023
Classification Class II
Status Ongoing
Quantity 26900 units
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
mislabeled
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Other
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2534-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[39814]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
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Reason for recall Ultrasound gel mislabeled with inappropriate use.
Code information a) 20-PMT03, Lot Numbers: 30479C3299 b) 20-PMT04, Lot Numbers: 30394C3279
Distribution pattern US, Canada, UK, Panama, Netherlands
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[6500]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 6
Procedural kits containing ultrasonic transmission gel, Item Numbers: a) 20-PC424, b) 20-PC448, c) 20-PC548, d) 20-PC596, e) 20-PC648
Z-2535-2023
Recall number Z-2535-2023
Initiated July 07, 2023
Classification Class II
Status Ongoing
Quantity 117875 units
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
mislabeled
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Other
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2535-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[39816]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Ultrasound gel mislabeled with inappropriate use.
Code information a) 20-PC424, Lot Numbers: 21109C2345; b) 20-PC448, Lot Numbers: 30371C3276; c) 20-PC548, Lot Numbers: 21088C2341, 30353C3268; d) 20-PC596, Lot Numbers: 20622C2244, 30481C3301; e) 20-PC648, Lot Numbers: 20145C2088, 20163C2097
Distribution pattern US, Canada, UK, Panama, Netherlands
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[6373]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 6
Procedural kits containing ultrasonic transmission gel, Item Numbers: a) 28-EG103, b) 28-EG125, c) 28-EG135, d) 28-EG151, e) 28-EG161, f) 28-EG163, g) 28-EG197
Z-2536-2023
Recall number Z-2536-2023
Initiated July 07, 2023
Classification Class II
Status Ongoing
Quantity 460 units
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
mislabeled
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Other
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2536-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[22674]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Ultrasound gel mislabeled with inappropriate use.
Code information a) 28-EG103, Lot Numbers: 10717C1190; b) 28-EG125, Lot Numbers: 30552C3318; c) 28-EG135, Lot Numbers: 10634C1175, 220221C2163; d) 28-EG151, Lot Numbers: 20655C2250, 20814C2279; e) 28-EG161, Lot Numbers: 10759C1198; f) 28-EG163, Lot Numbers: 10614C1166; g) 28-EG197, Lot Numbers: 10710C1190, 20804C2274;
Distribution pattern US, Canada, UK, Panama, Netherlands
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[6610]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 6
procedural kits containing ultrasonic transmission gel, Item Numbers: a)¿¿¿¿¿ 28-GG023, b)¿¿¿¿ 28-GG105, c)¿¿¿¿¿ 28-GG107, d)¿¿¿¿ 28-GG121, e)¿¿¿¿ 28-GG219, f)¿¿¿¿¿¿ 28-GG223, g)¿¿¿¿¿ 28-GG303, h)¿¿¿¿ 28-GG307, i)¿¿¿¿¿¿ 28-GG519, j)¿¿¿¿¿¿ 28-GG519PC, k)¿¿¿¿¿ 28-GG521, l)¿¿¿¿¿¿ 28-GG521PC, m)¿¿¿ 28-GG529, n)¿¿¿¿ 28-GG553, o)¿¿¿¿ 28-GG569, p)¿¿¿¿ 28-GG571, q)¿¿¿¿ 28-GG723
Z-2537-2023
Recall number Z-2537-2023
Initiated July 07, 2023
Classification Class II
Status Ongoing
Quantity 1880 units
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
mislabeled
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Other
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2537-2023
Source locator 0001-device-recall-0001-of-0001.json.zip#results[22675]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Ultrasound gel mislabeled with inappropriate use.
Code information a)¿¿¿¿¿ 28-GG023, Lot Numbers: 20794C0208; b)¿¿¿¿ 28-GG105, Lot Numbers: 21123C2346; c)¿¿¿¿¿ 28-GG107, Lot Numbers: 21039C2325; d)¿¿¿¿ 28-GG121, Lot Numbers: 21125C2346; e)¿¿¿¿ 28-GG219, Lot Numbers: 30440C2419; f)¿¿¿¿¿¿ 28-GG223, Lot Numbers: 21120C2341; g)¿¿¿¿¿ 28-GG303, Lot Numbers: 10484C1000; h)¿¿¿¿ 28-GG307, Lot Numbers: 20599C2238; i)¿¿¿¿¿¿ 28-GG519, Lot Numbers: 20599C2238; j)¿¿¿¿¿¿ 28-GG519PC, Lot Numbers: 20709C2256; k)¿¿¿¿¿ 28-GG521, Lot Numbers: 21126C2346; l)¿¿¿¿¿¿ 28-GG521PC, Lot Numbers: 21128C2346; m)¿¿¿ 28-GG529, Lot Numbers: 20783C0208; n)¿¿¿¿ 28-GG553, Lot Numbers: 10486C1000, 20816C2280; o)¿¿¿¿ 28-GG569, Lot Numbers: 21124C2346; p)¿¿¿¿ 28-GG571, Lot Numbers: 30502C2449; q)¿¿¿¿ 28-GG723, Lot Numbers: 30502C2449
Distribution pattern US, Canada, UK, Panama, Netherlands
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[6552]
FDA event record
· Exact recall-number query on openFDA
