- Recalling firm
- Angiodynamics, Inc.
- Reason for recall
- The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Distribution pattern
- Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon, Netherlands, New Zealand, Panama, Slovenia, South Africa, Spain, Sweden, Thailand.
- State
- NY
- Status
- Ongoing
- Recall number
- Z-1875-2026
- Recall initiated
- March 3, 2026