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Recall Observatory FDA recall evidence

Device product

SORIN GROUP, SMART PERFUSION PACK, SMART VENOUS VACUUM, REF 084118102, STERILE EO, Rx Only, 1 EA

Z-2787-2017

June 29, 2017

Class II

Product summary

Firm
Sorin Group USA, Inc.
Event
Event 77810
Status
Terminated
Classification
Class II
Quantity
632 units
Official record key
device-enforcement:Z-2787-2017

Official wording

Reason: Medtronic informed LivaNova that some of their DLP Pressure Disposable Display Sets are packaged in pouches which may have small pinholes (approximately 1mm or less in diameter). The result is a potential sterile barrier breach in the display sets. These display sets are included with LivaNova Perfusion Tube Sets (PTS) which were then distributed to customers.

Code information: Lot numbers: 1620200038, 1621700037, 1622800048, 1623100036, 1623700036, 1625700047, 1627900048, 1630500054, 1630600077, 1631900048, 1632700043, 1633500024, 1701000056, 1701600055, 1701800042 1704500037, 1705300070, 1706100042, 1707600055, 1706600103, 1707900056, 1708900035, 1710700038, 1712400062, 1713600042, 1714400058, 1715200088, 1715800067

Distribution pattern: Nationwide

Derived failure modes

  • Sterility assurance

    reason.sterility_assurance · v1.0.0

    sterile barrier breach