ClearanceBrief
Recall Z-1625-2011 ยท JDZ Mixer, Cement, For Clinical Use

Medtronic Spine LLC, formerly Kyphon Inc

Medtronic brand KyphX HV-R Bone Cement with Kyphon mixer, a polymethyl bone cement kit consisting of a quantity of powder (20 g) and a volume of liquid (10 ml/9 g) mixed in a Kyphon mixer for up to two minutes. Model Number: CO1B; Manufactured by Elmdown LTD, London, England, for Medtronic Spine LLC, Sunnyvale, CA. Product is a medical device used during balloon kyphoplasty to cement structures

DateMar 11, 2011 (initiated Nov 10, 2009)
StatusTerminated
ReasonProduct may not reach proper viscosity (dough state) and inconsistency or lack of homogeneity during cement preparation and during delivery period.
Root causeOther
ActionThe firm, Medtronic Spine LLC, sent an "URGENT DEVICE RECALL NOTICE" dated November 9, 2009 to the customers. The notice described the product, problem and actions to be taken. The customers were instructed to return the affected lots to Medtronic Spine; to not use any of the affected product that they may have received (Medtronic will replace any affected product in their inventory), the customer should contact their Medtronic Spine sales representative or customer service at [866-959-7466 or for geography] for assistance with replacement product, and complete and return the URGENT DEVICE REC
DistributionUSA including states of: AL, AR, AZ, CA, CO, DC, FL, GA, IA, IN, KY, MA, MD, MO, MT, NC, NM, NV, NY, OH, PA, SC, TN, TX, UT, VA, WI, and WV; and countries including: Argentina, Austria, Belgium, Brazil, Canada, Chile, Cyprus, Czech Republic, Denmark, Finland, France, Germany, Greece, Honduras, Hong
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K033801KYPHX HV-R, MODEL C01A
Kyphon, Inc., Apr 1, 2004
K041584KYPHX HV-R BONE CEMENT, MODEL C01A
Kyphon, Inc., Jul 7, 2004