Terumo Medical Corporation: Medical Device Recall in 2013 - (Recall #: Z-1611-2013)

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:

Pinnacle¿ Destination¿ Peripheral Guiding Sheath, 8 French, 90cm, Straight Tip, Cross Cut Valve. Acts as a conduit to facilitate the introduction of interventional and diagnostic devices into the human vasculature.

Product Classification:

Class II

Date Initiated: May 30, 2013

Date Posted: July 3, 2013

Recall Number: Z-1611-2013

Event ID: 65397

Reason for Recall:

Medical devices were incorrectly labeled with extended expiration dates.

Status: Terminated

Product Quantity: 20 units

Code Information:

Lot MM27

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated