Recall events
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Event 79146
Event summary
Timeline bucket September 13, 2017
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording Zimmer Biomet, 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
3 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 3
Phoenix Antegrade Femoral Nail Trochanteric and Piriformis fossa, Model#14-442093 Antegrade Femoral Connecting Bolt. orthopedic instrument
Z-0773-2018
Recall number Z-0773-2018
Initiated September 13, 2017
Classification Class II
Status Terminated
Quantity 337 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Fracture of the bolt connecting the insertion guide to the intramedullary nail during insertion of the femoral nail.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0773-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[34573]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Fracture of the bolt connecting the insertion guide to the intramedullary nail during insertion of the femoral nail.
Code information Finished Lot order: M370490 M354450 M321540 M975460 M639280 M426760 M629950 M629930 M073530 M073540 M073550 M073560 M073570 M073580 M073590 M073600 M073610 M627490 M656470 M656580 M656590 M656600 M656610 M656620 M656640 M656660 M966880 M967050 M967060 M967070 M980260 M980270 M508490 M508410 M508500 M508450 M508480 M508520 M508470 M508510 M508460
Distribution pattern Distribution includes 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[25805]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 3
14-442000S Antegrade Femoral Nail Instrument Kit, orthopedic instrument
Z-0774-2018
Recall number Z-0774-2018
Initiated September 13, 2017
Classification Class II
Status Terminated
Quantity 337 total
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Fracture of the bolt connecting the insertion guide to the intramedullary nail during insertion of the femoral nail.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0774-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[56878]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Fracture of the bolt connecting the insertion guide to the intramedullary nail during insertion of the femoral nail.
Code information Finished Lot order: M370490 M354450 M321540 M975460 M639280 M426760 M629950 M629930 M073530 M073540 M073550 M073560 M073570 M073580 M073590 M073600 M073610 M627490 M656470 M656580 M656590 M656600 M656610 M656620 M656640 M656660 M966880 M967050 M967060 M967070 M980260 M980270 M508490 M508410 M508500 M508450 M508480 M508520 M508470 M508510 M508460
Distribution pattern Distribution includes 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[25602]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 3
979195 Loaner Kit for femoral intramedullary nail. Orthopedic instrument.
Z-0775-2018
Recall number Z-0775-2018
Initiated September 13, 2017
Classification Class II
Status Terminated
Quantity 337 total
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Fracture of the bolt connecting the insertion guide to the intramedullary nail during insertion of the femoral nail.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0775-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[34575]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Fracture of the bolt connecting the insertion guide to the intramedullary nail during insertion of the femoral nail.
Code information Finished Lot order: M370490 M354450 M321540 M975460 M639280 M426760 M629950 M629930 M073530 M073540 M073550 M073560 M073570 M073580 M073590 M073600 M073610 M627490 M656470 M656580 M656590 M656600 M656610 M656620 M656640 M656660 M966880 M967050 M967060 M967070 M980260 M980270 M508490 M508410 M508500 M508450 M508480 M508520 M508470 M508510 M508460
Distribution pattern Distribution includes 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[25534]
FDA event record
· Exact recall-number query on openFDA
