Recall Z-0404-2011 ยท FRN Pump, Infusion
Angiodynamics, INC
Vortex LP, AngioDynamics, Inc., One Horizon Way, Manchester, GA 31816
| Date | Nov 17, 2010 (initiated Sep 27, 2010) |
| Status | Terminated |
| Reason | Labeling Error; The labeling for the specific products incorrectly identified that the packaged device kit contains a Lifeguard Safety Infusion Set. |
| Root cause | Other |
| Action | AngioDynamics issued a Notification of Medical Device Correction letter dated September 27, 2010 to customers. The notification served to make the customer aware of the mislabeling. Customers were instructed not to return the affected products. Customers can contact AngioDynamics at 1 800 772-6446 about this correction. |
| Quantity | see product one. |
| Distribution | Nationwide Distribution : Throughout the US. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K010767 | LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES Horizon Medical Products, Inc., Apr 10, 2001 |