ClearanceBrief
Recall Z-0834-2010 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

Becton Dickinson Medical Systems

BD Nexiva Closed IV Catheter System, REF 383536, 20GA 1.00IN, Becton Dickinson Infusion Therapy Systems Inc.

DateFeb 2, 2010 (initiated Oct 19, 2009)
StatusTerminated
ReasonManufacturing defect may allow air entry into a central venous catheter, possibly resulting in an air embolism.
Root causeProcess control
ActionConsignees were notified by B-D Urgent Medical Device Recall letter on 10/28/2009 and asked to return all unused affected lots. For information, call the company at 800-453-4538, option 2, extension 2341. Another letter was sent to all affected customers on 02/08/2010 notifying them of the extension of the recall to include Nexiva products. A response card was included to be returned whether or not product was on hand. B-D issued a press release on Febriuary 8, 2010. It can be found on www.bd.com at http://www.bd.com/contentmanager/b_article.asp?Item_ID=24486&ContentType_ID=1&BusinessCode=
Quantity1,021,600 units
DistributionNationwide distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K032843NEXIVA CLOSED IV CATHETER SYSTEM
Becton Dickinson Infusion Therapy Systems, Inc., Feb 27, 2004