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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 74986

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
August 08, 2016
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

2 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 2

Arterial Line Catheterization Kit with Sharps Safety Features Permits access to the peripheral arterial circulation or to other small vessels.

Z-2740-2016
Recall number
Z-2740-2016
Initiated
August 08, 2016
Classification
Class II
Status
Terminated
Recalling firm
Arrow International Inc
Quantity
690 kits

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
labeling error

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Shipping carton labeling error.

Code information

Device Listing # D025180

Distribution pattern

Nationwide Distribution to OH, IN, TN, NC, and KY.

device · product 2 of 2

Radial Artery Catheterization Kit with Sharps Safety Features Permits access to the peripheral arterial circulation. The safety feature is intended to help minimize the risk of sharps injuries when using the device.

Z-2741-2016
Recall number
Z-2741-2016
Initiated
August 08, 2016
Classification
Class II
Status
Terminated
Recalling firm
Arrow International Inc
Quantity
690 kits

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
labeling error

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Shipping carton labeling error.

Code information

Device Listing # D025180

Distribution pattern

Nationwide Distribution to OH, IN, TN, NC, and KY.