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Terumo Medical Corporation recalls Destination Guiding Sheath catheter introducer, Catalog Number: RSR06 Product Usage: The Destination¿ Guiding Sheath
Recalled March 7, 2018 · FDA recall Z-0725-2018 · Terumo Medical
Hazard
The tucking depth feature of this catheter introducer is marginally outside the upper specification. · FDA Class II
Units
33
Sold at
To be added.
Description
The tucking depth feature of this catheter introducer is marginally outside the upper specification.
Product
Destination Guiding Sheath catheter introducer, Catalog Number: RSR06 Product Usage: The Destination¿ Guiding Sheath is designed to be used for the introduction of interventional and diagnostic devices into the human vasculature, including but not limited to the renal, carotid, and peripheral arteries.
Manufacturer(s)
Terumo Medical Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →