ClearanceBrief
Recall Z-2103-2014 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

Terumo Cardiovascular Systems Corporation

Terumo TenderFlow Pediatric Venous Cannulae, 8, 10, 12, 14, 16, 18, 20, 22 & 24 Fr angled & straight tip, 1/4" & 3/8" flare, Product Usage: Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass surgery for dual cannulation of the superior and inferior vena cava

DateJul 23, 2014 (initiated May 23, 2014)
StatusTerminated
ReasonDuring an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS) identified the presence of loose fiber particulate that exceeded finished product specifications
Root causeProcess control
ActionTerumo sent an Urgent Medical Device Recall letters dated June 27, 2014 to their customers. The letter identified the affected product, problem and actions to be taken. The letter instructed customers to 1. Review this Medical Device Recall notice, 2. Assure that all users in your institution have received notice of this issue and remove any affected units from use, 3. Fill out the Product Tracking Sheet (enclosed), indicating the number of affected units at your institution and fax to 1-877-907-7509 or email to terumo4967@stericycle.com. 4. Complete the Packing Slip (enclosed) and follow
Quantity14,380 units
DistributionWorldwide Distribution - US (nationwide) in the states of: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY and the countries of : Australia, Bel
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K062597TENDERFLOW PEDIATRIC VENOUS RETURN CANNULA
Terumo Cardiovascular Systems Corp., Nov 3, 2006
K090878MODIFICATION TO TERUMO'S TENDERFLOW PEDIATRIC VENOUS RETURN CANNULAE (X-COATING)
Terumo Cardiovascular Systems Corp., Apr 3, 2009