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Recall Observatory FDA recall evidence

Device product

Pressure Monitoring sets with VAMP Plus closed blood sampling system model # T001691A, PXVP0566, PXVP2260, PXVP0826, PXVP0827, PXVP2284AT3, PXVP23X3AT3, T398807D, T100605B, T001762A, T391T00A, VP2. Blood sampling system used on patients requiring periodic withdrawal of blood samples.

Z-1146-2013

January 30, 2013

Class II

Product summary

Firm
Edwards Lifesciences, LLC
Event
Event 64229
Status
Terminated
Classification
Class II
Quantity
30,467
Official record key
device-enforcement:Z-1146-2013

Official wording

Reason: The device is being recalled because the firm has received multiple complaints related to incorrect assembly that may result in dilution of blood samples.

Code information: 59184554, 59187809, 59191725, 59221801, 59227844, 59238613, 59326333, 59356987, 59401041, 59222349, 59227178, 59234808, 59284693, 59328047, 59270408, 59284617, 59276238, 59401734, 59270380, 59319038, 59306624, 59390840, 59195810, 59331224, 59397181, 59291446, 59272771.

Distribution pattern: Worldwide Distribution-USA (nationwide) including the states of AR, CA, FL, HI, ID, IN, KS, KY, LA, MA, MI, MN, MO, NC, ND, NM, NV, NY, OH, OK, PA, SD, TN, TX, VA, WA, and WI) and Europe.

Derived failure modes

  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    incorrect assembly