FDA recall record

Terumo Custom Cardiovascular and Perfusion Procedure Kits Catalog Codes: Kits with a 5-digit recall — FDA Z-0159-2015

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.

Class IIclassification
Z-0159-2015official record ID
Nov 12, 2014report date

Recall record at a glance

Official recordZ-0159-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmTerumo Cardiovascular Systems Corp
Report dateNov 12, 2014
Recall initiation dateMar 1, 2011
QuantityCatalog Number: 6XXXX: 4561 units; Catalog Number: 7xxxx : 19356 units
LocationAshland, MA, United States

Official product description

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.

Why the product was recalled

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.

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

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