Recall events
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Event 96930
Event summary
Timeline bucket August 12, 2022
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording Chamberlain Technologies LLC
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
4 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 4
SURGIMESH WN, Polymeric Surgical Mesh, Large Flat Sheet, Model/Catalog Number: T3030
Z-1983-2025
Recall number Z-1983-2025
Initiated August 12, 2022
Classification Class II
Status Ongoing
Quantity 60 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Potential presence of residual adhesive material on the mesh surface.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1983-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17418]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Potential presence of residual adhesive material on the mesh surface.
Code information Lot Code: Reference Number: T3030 UDI: (01)00850011929186(17)250701(10)Z2459757F Lot Number: Z2459757F Expiration Date: 2025-07-01
Distribution pattern US distribution to states of: Illinois, Nebraska, & California
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[2695]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 4
SURGIMESH XB, Polymeric Surgical Mesh, 14m x 15cm Flat Sheet with Silicone Barrier, Model/Catalog Number: Tintra R-1415
Z-1984-2025
Recall number Z-1984-2025
Initiated August 12, 2022
Classification Class II
Status Ongoing
Quantity 20 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Potential presence of residual adhesive material on the mesh surface.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1984-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11589]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Potential presence of residual adhesive material on the mesh surface.
Code information Lot Code: Reference Number: Tintra R-1415 UDI: (01)00850011929032(17)250701(10)Z2459695M Lot Number: Z2459695M Expiration Date: 2025-07-01
Distribution pattern US distribution to states of: Illinois, Nebraska, & California
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[2700]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 4
SURGIMESH XB, Polymeric Surgical Mesh, X-Large Ellipse Barrier Mesh, Model/Catalog Number: Tintra E-3030
Z-1985-2025
Recall number Z-1985-2025
Initiated August 12, 2022
Classification Class II
Status Ongoing
Quantity 10 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Potential presence of residual adhesive material on the mesh surface.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1985-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29060]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Potential presence of residual adhesive material on the mesh surface.
Code information Lot Code: Reference Number: Tintra E-3030 UDI: (01)00850011929063(17)250701(10)Z2459757G Lot Number: Z2459757G Expiration Date: 2025-07-01
Distribution pattern US distribution to states of: Illinois, Nebraska, & California
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[2761]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 4
SURGIMESH WN, Polymeric Surgical Mesh, 14cm x 15cm Flat Sheet, Model/Catalog Number: T1415
Z-1986-2025
Recall number Z-1986-2025
Initiated August 12, 2022
Classification Class II
Status Ongoing
Quantity 20 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Potential presence of residual adhesive material on the mesh surface.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1986-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[23014]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Potential presence of residual adhesive material on the mesh surface.
Code information Lot Code: Reference Number: T1415 UDI: (01)00850011929155(17)250701(10)Z2459757H Lot Number: Z2459757H Expiration Date: 2025-07-01
Distribution pattern US distribution to states of: Illinois, Nebraska, & California
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[2724]
FDA event record
· Exact recall-number query on openFDA
