Recall events
/
Event 69644
Event summary
Timeline bucket October 17, 2014
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording Biomet Microfixation, 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
14 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 14
Total Temporomandibular Joint Replacement System- 45mm Lft Narrow Ti Mand
Z-0509-2015
Recall number Z-0509-2015
Initiated October 17, 2014
Classification Class II
Status Terminated
Quantity 42
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Laser etching on the parts is wider and deeper than the conditions previously validated.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software Design Change
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0509-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[2652]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Laser etching on the parts is wider and deeper than the conditions previously validated.
Code information Model 01-6546TI, Lot #s: 531880B, 535890B, 531870A, 531870B, 531880A, 535890D, 535890A, 535890C.
Distribution pattern Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.
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[23234]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 14
Total Temporomandibular Joint Replacement System- 45mm Lft Stand Off Ti Mand Reconstruction of the temporomandibular joint
Z-0510-2015
Recall number Z-0510-2015
Initiated October 17, 2014
Classification Class II
Status Terminated
Quantity 42
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Laser etching on the parts is wider and deeper than the conditions previously validated.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software Design Change
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0510-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[43289]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Laser etching on the parts is wider and deeper than the conditions previously validated.
Code information Models 24-6646TI, Lot #s: 526000A, 526000B, 526010B, 526010A, 535390A, 535390B, 535390C, 535390D, 538720A, 538720B, 538720C, 538720D
Distribution pattern Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.
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[24285]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 14
Total Temporomandibular Joint Replacement System- 45mm Rt Narrow Ti Mand Reconstruction of the temporomandibular joint
Z-0511-2015
Recall number Z-0511-2015
Initiated October 17, 2014
Classification Class II
Status Terminated
Quantity 42
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Laser etching on the parts is wider and deeper than the conditions previously validated.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software Design Change
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0511-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[55784]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Laser etching on the parts is wider and deeper than the conditions previously validated.
Code information Model 01-6545TI, Lot #s: 535380D, 531850A, 531850B, 531860A, 531860B, 535380B, 535380C, 535380A.
Distribution pattern Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.
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[23101]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 14
Total Temporomandibular Joint Replacement System- 45mm Rt Stand Off TI Mand Reconstruction of the temporomandibular joint
Z-0512-2015
Recall number Z-0512-2015
Initiated October 17, 2014
Classification Class II
Status Terminated
Quantity 42
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Laser etching on the parts is wider and deeper than the conditions previously validated.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software Design Change
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0512-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[49538]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Laser etching on the parts is wider and deeper than the conditions previously validated.
Code information Model 24-6645TI, Lot #s: 472580A, 472590B, 472580B, 472590A, 526030A, 526020A, 526020B, 526030B,
Distribution pattern Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.
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[24253]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 14
Total Temporomandibular Joint Replacement System- 50mm Lft Narrow Ti Mand Reconstruction of the temporomandibular joint
Z-0513-2015
Recall number Z-0513-2015
Initiated October 17, 2014
Classification Class II
Status Terminated
Quantity 42
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Laser etching on the parts is wider and deeper than the conditions previously validated.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software Design Change
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0513-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[49531]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Laser etching on the parts is wider and deeper than the conditions previously validated.
Code information Model 01-6551TI, Lot #s: 535370A, 535370B, 535370C, 535370D.
Distribution pattern Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.
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[23223]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 14
Total Temporomandibular Joint Replacement System- 50mm Lft Stand Off Ti Mand Reconstruction of the temporomandibular joint
Z-0514-2015
Recall number Z-0514-2015
Initiated October 17, 2014
Classification Class II
Status Terminated
Quantity 42
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Laser etching on the parts is wider and deeper than the conditions previously validated.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software Design Change
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0514-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[31886]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Laser etching on the parts is wider and deeper than the conditions previously validated.
Code information Model 24-6651TI, Lot #s: 472560A, 472560B, 472570A, 518520A, 518520B, 472570B.
Distribution pattern Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.
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[24113]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 14
Total Temporomandibular Joint Replacement System- 50mm Rt Narrow Ti Mand Reconstruction of the temporomandibular joint
Z-0515-2015
Recall number Z-0515-2015
Initiated October 17, 2014
Classification Class II
Status Terminated
Quantity 42
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Laser etching on the parts is wider and deeper than the conditions previously validated.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software Design Change
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0515-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[43296]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Laser etching on the parts is wider and deeper than the conditions previously validated.
Code information Model 01-6550TI, Lot #s: 531890A, 531890B, 531900A, 531900B, 544220B, 544230A, 544230B, 544200A, 544200B, 544210A, 544210B, 544220A.
Distribution pattern Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.
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[18229]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 14
Total Temporomandibular Joint Replacement System- 50mm Rt Stand Off Ti Mand Reconstruction of the temporomandibular joint
Z-0516-2015
Recall number Z-0516-2015
Initiated October 17, 2014
Classification Class II
Status Terminated
Quantity 42
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Laser etching on the parts is wider and deeper than the conditions previously validated.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software Design Change
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0516-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[14598]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Laser etching on the parts is wider and deeper than the conditions previously validated.
Code information Model 24-6650TI, Lot #s: 531960A, 531960B.
Distribution pattern Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.
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[23206]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 14
Total Temporomandibular Joint Replacement System- 50mm Rt Standard Ti Mand Reconstruction of the temporomandibular joint
Z-0517-2015
Recall number Z-0517-2015
Initiated October 17, 2014
Classification Class II
Status Terminated
Quantity 42
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Laser etching on the parts is wider and deeper than the conditions previously validated.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software Design Change
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0517-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[55783]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Laser etching on the parts is wider and deeper than the conditions previously validated.
Code information Model 24-6650TI, Lot #s: 518480B, 518480A, 525970A, 525970B, 525980B, 518490A, 526070A, 525990A, 525990B, 526060A, 526060B, 526070B, 525980A, 550330A, 550330B, 550340A, 550340B, 550350A, 550360A, 550360B, 518490B, 525960A, 525960B,
Distribution pattern Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.
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[24018]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-0518-2015
Initiated October 17, 2014
Classification Class II
Status Terminated
Quantity 42
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Laser etching on the parts is wider and deeper than the conditions previously validated.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software Design Change
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0518-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[14584]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Laser etching on the parts is wider and deeper than the conditions previously validated.
Code information Model 24-6551TI, Lot #s: 544160A, 525190A, 525190B, 525180B, 544170A, 544180B, 544160B, 525180A, 544180A.
Distribution pattern Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.
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[24056]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-0519-2015
Initiated October 17, 2014
Classification Class II
Status Terminated
Quantity 42
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Laser etching on the parts is wider and deeper than the conditions previously validated.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software Design Change
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0519-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[49539]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Laser etching on the parts is wider and deeper than the conditions previously validated.
Code information Model 24-6556TI, Lot #s: 520240A, 520230A, 550400A, 550390B, 520230B, 520240B, 535400B, 550400B, 535400A, 535410A, 535410B, 550370A, 550370B, 550380A, 550380B, 550390A.
Distribution pattern Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.
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[17324]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-0520-2015
Initiated October 17, 2014
Classification Class II
Status Terminated
Quantity 42
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Laser etching on the parts is wider and deeper than the conditions previously validated.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software Design Change
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0520-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[43294]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Laser etching on the parts is wider and deeper than the conditions previously validated.
Code information Model 24-6555TI, Lot #s: 525210B, 525200A, 525200B, 525210A.
Distribution pattern Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.
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[24096]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-0521-2015
Initiated October 17, 2014
Classification Class II
Status Terminated
Quantity 42
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Laser etching on the parts is wider and deeper than the conditions previously validated.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software Design Change
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0521-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[8096]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Laser etching on the parts is wider and deeper than the conditions previously validated.
Code information Model 24-6546TI, Lot #s: 526040B, 526050A, 526040A, 526050B.
Distribution pattern Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.
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[17310]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-0522-2015
Initiated October 17, 2014
Classification Class II
Status Terminated
Quantity 42
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Laser etching on the parts is wider and deeper than the conditions previously validated.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software Design Change
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0522-2015
Source locator 0001-device-recall-0001-of-0001.json.zip#results[24398]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Laser etching on the parts is wider and deeper than the conditions previously validated.
Code information Model 24-6545TI, Lot #s: 520220B, 520220A, 520210A, 520210B
Distribution pattern Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.
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[24106]
FDA event record
· Exact recall-number query on openFDA
