Exact FDA event identifier

Event 92702

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

Open FDA event record

Event summary

Timeline bucket: June 28, 2023
Product types: Device
Classifications: Class II
Statuses: Ongoing
Recalling firm wording: Medtronic Neurosurgery

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

Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter, STERILE EO, Rx Only

Z-2412-2023

Recall number: Z-2412-2023
Initiated: June 28, 2023
Classification: Class II
Status: Ongoing
Recalling firm: Medtronic Neurosurgery
Quantity: 44 units

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

labeling contains incorrect

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling Change Control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product labeling contains incorrect expiration date

Code information

Lot # 226632942; UDI-DI: 00763000624781

Distribution pattern

US Nationwide distribution in the states of NJ, FL, CA, IL.