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Recall Observatory FDA recall evidence

Device product

Sarns" Soft-Flow¿ Aortic Cannula without Suture Flange, straight tip, wire-reinforced with luer port, aortic cannula, 7.0 mm (21 Fr) OD with 3/8" connector, 14" (36 cm) long. Indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery.

Z-0194-2014

October 23, 2013

Class II

Product summary

Firm
Terumo Cardiovascular Systems Corporation
Event
Event 66624
Status
Terminated
Classification
Class II
Quantity
70 units
Official record key
device-enforcement:Z-0194-2014

Official wording

Reason: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS) identified the presence of loose fiber particulate that exceeded finished product specifications on certain product lots of Sarns" Soft-Flow¿ Aortic Cannulae and Sarns" Venous Return Cannulae.

Code information: Catalog Number 5798 Lot Numbers 0677301

Distribution pattern: Worldwide Distribution-USA including DC and the states of MO,TX,OK, LA, MA, CA, WI, and MI and the country of Canada.

Derived failure modes

  • Foreign material or chemical contamination

    reason.foreign_material_chemical_contamination · v1.0.0

    particulate