Exact FDA event identifier

Event 77917

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

Open FDA event record

Event summary

Timeline bucket: July 28, 2017
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Cardinal Health 200, 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

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

Convertors Robotic Drape with Attached Leggings; Product is packaged as Single Sterile Drape/8 per Case

Z-3046-2017

Recall number: Z-3046-2017
Initiated: July 28, 2017
Classification: Class II
Status: Terminated
Recalling firm: Cardinal Health 200, LLC
Quantity: 200 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Product 29474 LAVH drape was packaged as 29574 Robotic Drape with Leggings.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product 29474 LAVH drape was packaged as 29574 Robotic Drape with Leggings.

Code information

Lot number 17DAH349

Distribution pattern

US Distribution to the states of : NC, UT, OR, NY,TX, GA, NJ and FL.