Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MicroStic Plus w/SS Wire 5F and MicroStic Plus w/NiTi Wire Recalled by Argon Medical Devices, Inc Due to The supplier initiated a recall because affected lots...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Argon Medical Devices, Inc directly.
Affected Products
MicroStic Plus w/SS Wire 5F and MicroStic Plus w/NiTi Wire & Echo Needle 4F. A sheath used to facilitate placing a catheter through the skin into a vein or artery.
Quantity: 200 units
Why Was This Recalled?
The supplier initiated a recall because affected lots of the micro-introducer have an outer diameter of the dilator hub that is slightly smaller than is capable of securing the dilator to the sheath
Where Was This Sold?
This product was distributed to 2 states: MS, TN
About Argon Medical Devices, Inc
Argon Medical Devices, Inc has 42 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report