Exact FDA event identifier

Event 77592

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket: June 23, 2017
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Exactech, 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

1 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 1

Truliant Tibial Trial Handle. To assist the surgeon in the implantation of Truliant Knee system components according to a conventional technique for total knee replacement. Specifically, these instruments are reusable, surgically invasive, and intended for transient use.t Tibial Trial Handle

Z-3018-2017

Recall number: Z-3018-2017
Initiated: June 23, 2017
Classification: Class II
Status: Terminated
Recalling firm: Exactech, Inc.
Quantity: 68 devices

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

The Truliant Tibial Trial Handle's pin may disassociate from the main body.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Truliant Tibial Trial Handle's pin may disassociate from the main body.

Code information

Catalog Number 02-029-29-1000, Lot Number 83843-001.

Distribution pattern

US Distribution to the states of : AZ, CA, CO, FL, IL, OH, OK, NV, NY, SC and TN.