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Argon Medical Devices, Inc recalls ClosureFast Micro Introducer Sheath Set, REF MIS-7F11; 7Fr/Ch (2.3mm)x11 cm. STERILE|EO; Rx ONLY - Product Usage: Introd
Recalled August 26, 2020 · FDA recall Z-2806-2020 · Argon Medical Devices
Hazard
Sterile introducer sheath set manufactured under one lot with different expiration dates. · FDA Class II
Units
1000 units
Sold at
US Nationwide distribution including in the state of MS.
Description
Sterile introducer sheath set manufactured under one lot with different expiration dates.
Product
ClosureFast Micro Introducer Sheath Set, REF MIS-7F11; 7Fr/Ch (2.3mm)x11 cm. STERILE|EO; Rx ONLY - Product Usage: Introducer Products are stand-alone components, standard kits, or convenience kits built to user specifications. These products facilitate access to a vein or artery, allowing various catheters to be passed through for local or central diagnostic or therapeutic interventions. Indicated for use in arterial and venous procedures requiring percutaneous introduction of intravascular devices.
Manufacturer(s)
Argon Medical Devices, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →