Medrad Inc: 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 Medrad Inc 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:

DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris MR Vital Signs Monitor: Product Usage: Monitor, Physiological, Patient
MEDRAD Hand Controller Sheath, Catalog number AVA 500 HCS/3010903, for cardiac catheterization procedures. The Sterile Sheath is specifically intended for use in the x-ray angiography environment to cover the Medrad Avanta Sterile Hand Controller to prevent cross contamination between patients.