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Recall

Class II — Terumo Cardiovascular Systems Corporation

Recalling firmTERUMO CARDIOVASCULAR SYSTEMS CORP.
Registered facilityTERUMO CARDIOVASCULAR SYSTEMS CORPORATION (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonDuring set-up and priming of the bypass circuit, leaks were detected on the centrifugal pumphead.
ProductCardiovascular Procedure Kit containing Disposable Centrifugal Pumphead with or without X-Coating, sterile single use. Catalog numbers 73431, 73813-03, 74277, 72481-01, 72427, 70947-03, 74570-01, 74031-01, 73312-01, 74362, 74928, 74928-01, 72997-03, 74277, 70334-03, 73230, 73728, 71537, 73605-01, 74482-01, 74857-01, 74916, 73928-02, 70123-02, 71853-02, 72997-03, 74766, 71537, 73728, 72269, 74466, 71317-02 72991-02, 74951, 74336, 74121-01, 72941-01, 73315-03, 74559, 74277, 71382-01, 73108-02, 74178-03, 71598-02, 73108-02, 74618-01, 70334-03, 74802-01, 74916, 71932-02, 7095…
Quantity256 kits
DistributionNationwide Distribution
Initiated2014-04-14
Classified2014-07-11
Terminated2016-09-07
Recall numberZ-2030-2014
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Terumo Cardiovascular Systems Corporation (Z-2030-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/68024/

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