Sorin Group USA, Inc.: Medical Device Recall in 2017 - (Recall #: Z-2785-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

SORIN GROUP, SMART PERFUSION PACK, SMA PRIMO2X OPTI PACK, REF 088512900, STERILE EO, Rx Only, 1 EA

Product Classification:

Class II

Date Initiated: June 29, 2017

Date Posted: August 9, 2017

Recall Number: Z-2785-2017

Event ID: 77810

Reason for Recall:

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.

Status: Terminated

Product Quantity: 524 units

Code Information:

Lot Numbers: 1620700048, 1621600063, 1623700039, 1624500038, 1625900047, 1626500084, 1627800066, 1628500062, 1630000040, 1630500055, 1631400035, 1633300052, 1635400049, 1700600038, 1702500069, 1704500039, 1706600107, 1707400082, 1708600072, 1710800102, 1711700034, 1713600045, 1715000038, 1717000046

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated