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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 62125

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

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Event summary

Timeline bucket
June 07, 2012
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Arrow International 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

Arrow International, Inc. 7FR 3-Lumen Arrowg+ard Blue Plus(R) Pressure Injectable Central Venous Catheter - Catalog number CDC-42703-XP1A The multiple-lumen pressure injectable catheter permits venous access to central circulation and injection of contrast media. The ARROWg+ard(R) antimicrobial surface is intended to provide protection against catheter-related infections.

Z-1823-2012
Recall number
Z-1823-2012
Initiated
June 07, 2012
Classification
Class II
Status
Terminated
Recalling firm
Arrow International Inc
Quantity
1,085

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arrow is recalling the product due to the possibility of voids in the catheter hub which could lead to an interlumen crossover.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arrow is recalling the product due to the possibility of voids in the catheter hub which could lead to an interlumen crossover.

Code information

Lot number RF2033361

Distribution pattern

USA (nationwide) AL, AZ, AR, CA, CO, FL, GA, IL, IN, KS, LA, MA, MI, MO, NV, NH, NC, OH, PA, TX, VA, WA, and WI.