Terumo Cardiovascular Systems Corporation: Medical Device Recall in 2014 - (Recall #: Z-1069-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System, Part number: VSP550, Sterile***Rx Only*** Product Usage: The VirtuoSaph Plus Endoscopic Vessel Harvesting System is indicated for use in minimally invasive surgery allowing access for vessel harvesting, and is primarily indicated for patients undergoing endoscopic surgery for arterial bypass.

Product Classification:

Class II

Date Initiated: December 12, 2013

Date Posted: March 5, 2014

Recall Number: Z-1069-2014

Event ID: 67193

Reason for Recall:

Sterility of medical devices intended for use in surgical procedures may be compromised.

Status: Terminated

Product Quantity: 26 units

Code Information:

Lot numbers: 21K, 31K, 32K, 33K, 34K, 35K

Distribution Pattern:

USA Nationwide Distribution in the state of LA, NJ, and NY.

Voluntary or Mandated:

Voluntary: Firm initiated