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Sorin C5 System Model 58-00-00

by Sorin Group Deutschland GmbH

510(k) K093882

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

7 closed

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 11 Oct 2026. What this means

Regulatory status

as of registry sync 11 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Special NumberK093882 Date15 Jan 2010ClearedStatusActive

Recalls

7 recalls · FDA

    • Terminated Z-0856-2014 FDA Class II initiated 4 Dec 2013

    Sorin is initiating a field correction on S5/C5 Heart-lung machine and CP5 centrifugal pump system due to reports of pump speed control knob failures resulting in no response.

    • Terminated Z-0271-2013 FDA Class II initiated 19 Sep 2012

    Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding certain serial numbers of the Sorin Group S5 Perfusion System due to reports of a "Fault in motor controller" alarm message displayed on the system panel. This could lead to unintended pump stoppage which may result in permanent impairment or life-threatening injury. An out of specification electrical component was determi

  • 4 recalls, same reason

    • Terminated Z-0272-2013 FDA Class II initiated 19 Sep 2012
    • Terminated Z-0275-2013 FDA Class II initiated 19 Sep 2012
    • Terminated Z-0274-2013 FDA Class II initiated 19 Sep 2012
    • Terminated Z-0273-2013 FDA Class II initiated 19 Sep 2012

    Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding certain serial numbers of the Sorin Group S5 Perfusion System due to reports of a "Fault in motor controller" alarm message displayed on the system panel. This could lead to unintended pump stoppage which may result in permanent impairment or life-threatening injury. An out of specification electrical component was determin

    • Terminated Z-1330-2012 FDA Not yet classified initiated 23 Feb 2012

    The pump speed control knob is attached to the shaft of an encoder that is used to adjust the speed. Insufficient lubrication within the encoder increases friction over time making it more difficult to turn the pump speed control knob. Excessive friction causes premature wear of the encoder shaft which can result in a stuck shaft.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
DTQ
Device Class
Class II
Regulation
21 CFR Part 870.4220
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

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