Exact FDA event identifier

Event 71260

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

Open FDA event record

Event summary

Timeline bucket: May 21, 2015
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Baxter Healthcare Corp

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

ONE-LINK NON-DEHP Y-TYPE MICROBORE CATHETER EXTENSION SET NEEDLE-FREE IV CONNECTOR WITH NEUTRAL FLUID DISPLACEMENT

Z-0132-2016

Recall number: Z-0132-2016
Initiated: May 21, 2015
Classification: Class II
Status: Terminated
Recalling firm: Baxter Healthcare Corp
Quantity: 23,600

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Potential for a leak at the tubing to luer bond.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for a leak at the tubing to luer bond.

Code information

Code: 7N8371, Lots: UR15B16021 and UR15B23043

Distribution pattern

Domestic Only