Recall events
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Event 69723
Event summary
Timeline bucket November 24, 2014
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording Arthrosurface, 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
5 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 5
Arthrosurface 25&30mm 10.5x28mm Taper Post Fixation Component; Catalog Number: 6105-0028, Pat Number 1105-0028. HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing. Orthopedic shoulder prosthesis component.
Z-1110-2015
Recall number Z-1110-2015
Initiated November 24, 2014
Classification Class II
Status Terminated
Quantity 136
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications.
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-1110-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[7856]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications.
Code information Catalog Number: 6105-0028, Part Number 1105-0028
Distribution pattern Worldwide Distribution - USA nationwide. Internationally distributed to Europe, Canada, and Australia. Only products in US affected by this recall.
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[23515]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 5
Arthrosurface 25&30mm 12.5x32mm Taper Post Fixation Component; Catalog Number: 6125-0035, Part Number: 1125-0035. HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing. Orthopedic shoulder prosthesis component.
Z-1111-2015
Recall number Z-1111-2015
Initiated November 24, 2014
Classification Class II
Status Terminated
Quantity 143
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications.
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-1111-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[14317]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications.
Code information Catalog Number: 6125-0035, Part Number: 1125-0035
Distribution pattern Worldwide Distribution - USA nationwide. Internationally distributed to Europe, Canada, and Australia. Only products in US affected by this recall.
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[23133]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 5
Arthrosurface 35mm 13.5x32mm Taper Post Fixation Component; Catalog Number: 8135-0032, Part Number: 3135-0032. HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing. Orthopedic shoulder prosthesis component.
Z-1112-2015
Recall number Z-1112-2015
Initiated November 24, 2014
Classification Class II
Status Terminated
Quantity 138
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications.
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-1112-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32198]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications.
Code information Catalog Number: 8135-0032, Part Number: 3135-0032
Distribution pattern Worldwide Distribution - USA nationwide. Internationally distributed to Europe, Canada, and Australia. Only products in US affected by this recall.
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[18325]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 5
Athrosurface 40mm 13.75x31mm Taper Post Fixation Component; Catalog Number: 8135-1875 Part Number: 3135-1875. HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing. Orthopedic shoulder prosthesis component.
Z-1113-2015
Recall number Z-1113-2015
Initiated November 24, 2014
Classification Class II
Status Terminated
Quantity 182 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications.
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-1113-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[49705]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications.
Code information Catalog Number: 8135-1875 Part Number: 3135-1875
Distribution pattern Worldwide Distribution - USA nationwide. Internationally distributed to Europe, Canada, and Australia. Only products in US affected by this recall.
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[18329]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 5
Arthrosurface HHXL (OVO) 15.6x32mm Taper Post Fixation Component; Catalog Number: 8156-0032, Part Number: 156-0032. HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing. Orthopedic shoulder prosthesis component.
Z-1114-2015
Recall number Z-1114-2015
Initiated November 24, 2014
Classification Class II
Status Terminated
Quantity 187
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications.
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-1114-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[24383]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications.
Code information Catalog Number: 8156-0032, Part Number: 156-0032
Distribution pattern Worldwide Distribution - USA nationwide. Internationally distributed to Europe, Canada, and Australia. Only products in US affected by this recall.
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[18318]
FDA event record
· Exact recall-number query on openFDA
