Medical device recalls Moderate risk

Terumo Cardiovascular Systems Corp recalls Terumo Custom Cardiovascular Procedure Kit X-Coated Perfusion Pack P/N: 74077-01 Terumo Cardiovascular Procedure Kits a…

Recall date
August 24, 2015
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2790-2015
FDA classification
Class II
Brand / firm
Terumo Cardiovascular Systems Corp
Sold / distributed
Nationwide Distribution including CA, CT , FL , WI.

Why it was recalled

Custom Cardiovascular Procedure Kits contain recalled component Medivators HPH700 High Performance Hemoconcentrators

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Terumo Custom Cardiovascular Procedure Kit X-Coated Perfusion Pack P/N: 74077-01 Terumo Cardiovascular Procedure Kits are manufactured and customized to the design and specifications of the purchaser and/or the purchaser's principal technical representative for the application intended by the end user. The kits are comprised of a variety of legally marketed medical devices [including Medivators HPH700 High Performance Hemoconcentrators]. The Hemocor HPH700 Hemoconcentrator is intended for use as an ultrafiltration system to remove excess fluid during and/or following cardiopulmonary bypass procedures where acute hemodilution has been employed

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