Argon Medical Devices, Inc Hydrophilic Guidewire, Catalog Number: TVS3010, .035/150 cm, regular/angled/standard, sold as a single hydrophilic guidewire in sterile packaging. Total Vein Solutions, 901 Yale Street - Houston, Texas 77008, (713) 863-1600 Fax 713 863-1601, www.totalvein.com. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Hydrophilic Guidewire, Catalog Number: TVS3010, .035/150 cm, regular/angled/standard, sold as a single hydrophilic guidewire in sterile packaging. Total Vein Solutions, 901 Yale Street - Houston, Texas 77008, (713) 863-1600 Fax 713 863-1601, www.totalvein.com.
Brand
Argon Medical Devices, Inc
Lot Codes / Batch Numbers
All lot codes.
Products Sold
All lot codes.
Argon Medical Devices, Inc is recalling Hydrophilic Guidewire, Catalog Number: TVS3010, .035/150 cm, regular/angled/standard, sold as a sing due to Hydrophilic guidewires have the potential to demonstrate degradation of the Pebax cladding.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Hydrophilic guidewires have the potential to demonstrate degradation of the Pebax cladding.
Recommended Action
Per FDA guidance
Argon Medical Devices Inc. issued an "Urgent Field Safety Notice" letter dated February 26, 2009 informing all consignees of the affected product. Consumers were asked to immediately quarantine and return any product remaining followed by completion and return of the provided response form via email or fax (1-903-677-9396). For further questions or additional information call Argon Medical Devices Inc. at 1-903-677-9319.
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
AL, CA, CO, FL, GA, IL, KS, LA, MA, MI, MN, MO, MT, NV, NJ, NY, NC, PA, SC, TN, TX, UT, VA, WI, PR
Page updated: Jan 10, 2026