Sorin Group USA, Inc.: Medical Device Recall in 2017 - (Recall #: Z-2784-2017)

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, SMART CIRCULATORY ASSIST PACK, REF 627255003, STERILE EO, Rx Only, 1 EA

Product Classification:

Class II

Date Initiated: June 29, 2017

Date Posted: August 9, 2017

Recall Number: Z-2784-2017

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: 98 units

Code Information:

Lot Numbers: 1620000123, 1622800056, 1623500052m 1627700083, 1631200074, 1700300040, 1701000065, 1703700061, 1706500063, 1708000068, 1717000057

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated