FDA Enforcement Class II Ongoing

MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-767

Recall: Z-1344-2024 · Reported March 27, 2024

Enforcement

Recall Number
Z-1344-2024
Event ID
94035
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Angiodynamics, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
March 27, 2024
Initiation Date
January 30, 2024
Classification Date
March 21, 2024
Address
603 Queensbury Ave, Queensbury, NY, 12804-7619, United States

Description

MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-767

Reason

Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case

Code Info

UDI: 15051684023108 UPN: H965457671 Lot Number: 5787806 5790679 5795962 5803521 5806728

Distribution

Worldwide distribution - US Nationwide and the countries of AT, CA, CH, CZ, ES, HK, KW, NL, NO, NZ, ZA.

Quantity

200 units