Recall events
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Event 79242
Event summary
Timeline bucket June 30, 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
2 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 2
DELTA CER FEM HD 32/0MM T1 Product Usage: For use in hip arthroplasty
Z-0992-2018
Recall number Z-0992-2018
Initiated June 30, 2017
Classification Class II
Status Terminated
Quantity 30
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product may contain the presence of melted sterile packaging upon opening.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Packaging process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0992-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[45908]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Product may contain the presence of melted sterile packaging upon opening.
Code information part number: 650-1162 lot number: 2016030466
Distribution pattern US in the state of Texas
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[9596]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 2
JUGGERKNOT 2.9MM 2 #2 MB Product Usage: For use in hip arthroplasty
Z-0993-2018
Recall number Z-0993-2018
Initiated June 30, 2017
Classification Class II
Status Terminated
Quantity 50
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
For soft tissue fixation
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Packaging process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0993-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[56355]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall For soft tissue fixation
Code information Part number: 912050 Lot number: 221890
Distribution pattern US in the state of Texas
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[8958]
FDA event record
· Exact recall-number query on openFDA
