Terumo Medical Corporation: Medical Device Recalls in 2013

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Terumo Medical Corporation in 2013. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

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.
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.