Recall Z-1702-2016 ยท DWE Tubing, Pump, Cardiopulmonary Bypass
Angiodynamics Inc. (Navilyst Medical Inc.)
AngioVac Circuit Pack (Tandem Packs), REF/Catalog No. 25-187, UPN H965251870, STERILE, Rx Only, Single Use Only -- The AngioVac Circuit and AngioVac Circuit Pack are designed to be used with the AngioVac Cannula.
| Date | May 20, 2016 (initiated Mar 21, 2016) |
| Status | Terminated |
| Reason | Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump, determined that the products may possess levels of endotoxin that exceed regulatory limits. AngioDynamics confirmed that the affected RotaFlow Centrifugal Pumps were included in packaged AngioVac Circuit Packs. |
| Root cause | Environmental control |
| Action | On 3/21/2016, AngioDynamics sent recall notification packages (dated 3/21/2016) to the consignees via Federal Express. Consignees are instructed to follow the instructions provided on the Maquet Cardiopulmonary recall letter (dated 2/23/2016) and return the Reply Verification Tracking Form, provided in the recall notification. |
| Quantity | Domestic: 377 kits |
| Distribution | Nationwide Distribution. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K142607 | AngioVac Circuit Angiodynamics, Dec 11, 2014 |