Terumo Medical Corporation: Medical Device Recall in 2013 - (Recall #: Z-1612-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Terumo Glidesheath (tm), 6 French, Nitinol wire, product code 15-1060. Used to facilitate placing a catheter through the skin into a vein or artery.

Product Classification:

Class II

Date Initiated: May 30, 2013

Date Posted: July 3, 2013

Recall Number: Z-1612-2013

Event ID: 65397

Reason for Recall:

Medical devices were incorrectly labeled with extended expiration dates.

Status: Terminated

Product Quantity: 550 units

Code Information:

Lot MP08

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated