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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 69072

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

Open FDA event record

Event summary

Timeline bucket
August 11, 2014
Product types
Device
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Datascope Corporation

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

LINEAR 7.5 FR. 40cc IAB Catheter Maquet Getinge Group

Z-2568-2014
Recall number
Z-2568-2014
Initiated
August 11, 2014
Classification
Class III
Status
Terminated
Recalling firm
Datascope Corporation
Quantity
one unit

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
During label reconciliation a duplicate serial number label was detected to be printed for the LINEAR 7.5 FR 40 cc Intra-Aortic Balloon Catheter.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling False and Misleading

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

During label reconciliation a duplicate serial number label was detected to be printed for the LINEAR 7.5 FR 40 cc Intra-Aortic Balloon Catheter.

Code information

Part Number - 0684-00-0480-01U

Distribution pattern

US Distribution to TX.