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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 80378

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

Open FDA event record

Event summary

Timeline bucket
May 23, 2018
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

Percutaneous Sheath Introducer Kit for use with 7 - 7.5 Fr. Catheters (8 Fr. 10 cm sheath length .035 inch dia. spring-wire guide), REF ES-09807. The percutaneous sheath introducer permits venous access and catheter introduction to the central circulation.

Z-2576-2018
Recall number
Z-2576-2018
Initiated
May 23, 2018
Classification
Class II
Status
Terminated
Recalling firm
Arrow International Inc
Quantity
60 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product contains dry natural rubber latex. Label states Latex Free.

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

Product contains dry natural rubber latex. Label states Latex Free.

Code information

Lot/Batch Number: 13F18A0037 Expiration Date/Expected Life: Apr 2019

Distribution pattern

Puerto Rico