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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 62471

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

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Event summary

Timeline bucket
May 29, 2012
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Maquet 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

Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG Kehler Strabe 31 76437 Rastatt Germany Phone +49 7222 932-0 Fax: +49 7222 932-1888 info.cp@maquet.com www.maquet.com Used to introduce blood and sterile solution to the circulation system during extracorporeal circulation procedures

Z-2210-2012
Recall number
Z-2210-2012
Initiated
May 29, 2012
Classification
Class II
Status
Terminated
Recalling firm
Maquet Inc.
Quantity
20 devices US; 122 devices foreign

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Certain pediatric arterial cannulas may have limited flexibility due to an increased length of the "hardened" cannula tip.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

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Inspect official wording and provenance

Reason for recall

Certain pediatric arterial cannulas may have limited flexibility due to an increased length of the "hardened" cannula tip.

Code information

510k023251 US Catalog Number 161412 Batch Number 92048923 Foreign Catalog number 161412 Batch number 92048923 Catalog number 161412 Batch number 92051578

Distribution pattern

Worldwide Distribution - USA including MI, MN and Internationally

Field note

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