ClearanceBrief
Recall Z-1076-05 ยท IZI System, X-Ray, Angiographic

Argon Medical Devices, Inc

Product consists of a syringe used to inject fluids during an angiographic procedure for fluoroscopic imaging. Labeling is as follows: Product Label ''***Argon Medical Device***10cc Control Syringe FR/TR/FM w/ Reservoir SINGLE USE ONLY***REF/REORDER NO. 093205***This device is designed for the administration and removal of fluids***Quantity: 25ea***NON-STERILE*FURTHER PROCESSING REQUIRED***Eto (e

DateAug 3, 2005 (initiated Jun 27, 2005)
StatusTerminated
ReasonThe firm is recalling the product due to the potential for air aspiration or fluid leakage from a faulty syringe tip.
Root causeOther
ActionThe firm plans to distribute recall letters to all customers indicated on the customer list. TELEPHONE 6/27/2005. All products will be returned to Argon and disposed.
Quantity1008 syringes
DistributionTN, IL, WI, MA, VA, IN, LA, TX, CA, JAPAN, GERMANY, THE NETHERLANDS
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K911732ADVANCE DISPOSABLE CONTROL SYRINGE
Advance Medical Designs, Inc., Sep 16, 1991