Home / Recalls / Medical Devices
Terumo Medical Corp recalls MISAGO RX Self Expanding Peripheral Stem
Recalled December 7, 2016 · FDA recall Z-0669-2017 · Terumo Medical
Hazard
During recent routine testing, the MISAGO Peripheral Stent was found not to conform to product specification related to stent diameter at the proximal/distal ends and/or the shape of the stent. · FDA Class II
Units
7,965 units
Sold at
Nationwide
Description
During recent routine testing, the MISAGO Peripheral Stent was found not to conform to product specification related to stent diameter at the proximal/distal ends and/or the shape of the stent.
Product
MISAGO RX Self Expanding Peripheral Stem
Manufacturer(s)
Terumo Medical Corp
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →