Recalls / —
—#113707
Product
24 Fr 8mm Sft Flow Straight The Sarns Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use.
- FDA product code
- DWF — Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
- Device class
- Class 2
- Medical specialty
- Cardiovascular
- 510(k) numbers
- K934127
- Affected lot / code info
- catalog number: 5847 and lot number: 0582251 and 0586068
Why it was recalled
The presence of plastic flash was identified at the tip of certain lots of Sarns Soft-Flow Aortic Cannula. The plastic flash has the potential to detach and contribute to an adverse patient effect. While this potential failure has not been reported from the field as an observed defect, it was determined that the product does not meet specifications and this condition could result in an unacceptabl
Root cause (FDA determination)
Process design
Action the firm took
TERUMO sent an URGENT MEDICAL DEVICE RECALL letter dated September 20, 2012, to all affected customers. The letter identified the product, the problem, and the aciton to be taken by the customer. Customers were instructed to remove this cannulae from circulation and return them for credit. Customers with questions should call 1-800-521-2818. For questions regarding this recall call 734-741-6173.
Recalling firm
- Firm
- Terumo Cardiovascular Systems Corporation
- Address
- 6200 Jackson Road, Ann Arbor, Michigan 48103-9586
Distribution
- Distribution pattern
- Worldwide Distribution - USA including AL , CA , CO , DC , DE , FL , GA , IL , IN , KS , KY , LA , MA , MI , MO , MS , MT , NC , ND , NE , NH , NY , OH , PA , TN , TX , VA , and WI. Internationally to Australia, United Arab Emirates (UAE), Singapore, Malaysia, BELGIUM, Japan, and CANADA.
Timeline
- Recall initiated
- 2012-11-21
- Posted by FDA
- 2012-12-03
- Terminated
- 2013-04-23
- Status
- —
Source: openFDA Device Recall endpoint. Recall record ID #113707. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.