ProductGuru Recalls

Official recall record

Mini-Stick Max Coaxial Microintroducer Kit

Health Canada — Medical Devices · 2024-02-09 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2024-02-09
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

Angiodynamics, Inc., is conducting a medical device field safety corrective action (FSCA) to the end user level based on the non-conformance of a supplied component included within the Angiodynamics Mini Stick Max Coaxial Microintroducer Kit. This 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. Recall start date: January 30, 2024

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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