Argon Medical Devices, Inc Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, Catalog Number: AG087301, .035/150cm, regular/straight/standard, sold as a single hydrophilic guidewire in bulk non-sterile packaging. Argon Medical Devices, Inc. Athens, TX 75751. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, Catalog Number: AG087301, .035/150cm, regular/straight/standard, sold as a single hydrophilic guidewire in bulk non-sterile packaging. Argon Medical Devices, Inc. Athens, TX 75751.
Brand
Argon Medical Devices, Inc
Lot Codes / Batch Numbers
All lot codes.
Products Sold
All lot codes.
Argon Medical Devices, Inc is recalling Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, Catalog Number: AG087301, .035/150cm, r 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