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Recall Observatory FDA recall evidence

Device product

Terumo Custom Cardiovascular and Perfusion Procedure Kits Catalog Codes: Kits with a 5-digit code beginning with the digit 6: Catalog Number: 6XXXX ; Catalog Codes: Kits with a 5-digit code beginning with the digit 7: Catalog Number: 7XXXX Product usage: The Cardioplegia Delivery Sets are indicated for delivery of cardioplegic solutions to the heart during cardiopulmonary bypass surgery. The Cardiovascular Procedure Kits are indicated for use only in the extracorporeal circuit for the cardiopulmonary bypass procedure(s) for which the user designed it.

Z-0159-2015

March 01, 2011

Class II

Product summary

Firm
Terumo Cardiovascular Systems Corp
Event
Event 58185
Status
Terminated
Classification
Class II
Quantity
Catalog Number: 6XXXX: 4561 units; Catalog Number: 7xxxx : 19356 units
Official record key
device-enforcement:Z-0159-2015

Official wording

Reason: Defect in the luer connector can compromise the seal on the female side of the connector and the compromised seal can introduce air in the table line.

Code information: Catalog Number: 6XXXX Lot Numbers: ML07, MM18, MM25, MN08, MN IS, MN22. Manufacturing dates September 7, 20 I 0 through November 22, 20 I 0. Catalog Number: 7XXXX Lot Numbers: ML07,ML20, MM18, MM25, MNO1, MN08, MN15, MN29,MP06, MP13. Manufacturing dates September 7, 2010 through December 13,2010.

Distribution pattern: Worldwide Distribution: US (nationwide) and the countries of Canada, Brazil, Hong Kong, Korea, and Thailand.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Defect in the luer connector can compromise the seal on the female side of the connector and the compromised seal can introduce air in the table line.