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 (ethylene oxide) Sterilization Recommended***1445 FLAT CREEK ROAD - ATHENS, TX 75751***800-927-4669*** Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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 (ethylene oxide) Sterilization Recommended***1445 FLAT CREEK ROAD - ATHENS, TX 75751***800-927-4669***
Brand
Argon Medical Devices, Inc
Lot Codes / Batch Numbers
Reorder #: 00-093207 - Lot #: 99442547
Products Sold
Reorder #: 00-093207 - Lot #: 99442547
Argon Medical Devices, Inc is recalling Product consists of a syringe used to inject fluids during an angiographic procedure for fluoroscopi due to The firm is recalling the product due to the potential for air aspiration or fluid leakage from a faulty syringe tip.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The firm is recalling the product due to the potential for air aspiration or fluid leakage from a faulty syringe tip.
Recommended Action
Per FDA guidance
The 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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, IL, IN, LA, MA, TN, TX, VA, WI
Page updated: Jan 10, 2026