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Angiodynamics, Inc.

Angiodynamics, Inc. Recalls

All product recalls associated with Angiodynamics, Inc..

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Feb 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 21–28 of 28 recalls

Angiodynamics, Inc.: MINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO 1.6" PG- U...

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

Moderate

FDAJan 30, 2024Nationwide• Angiodynamics, Inc.

Angiodynamics, Inc.: MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS ECHO 2.75" PG-...

Moderate

FDAJan 30, 2024Nationwide• Angiodynamics, Inc.

Angiodynamics, Inc.: MINI STICK MAX 5F X 10 CM STIFF .018 SS/PD ECHO 2.75" PG-...

Page 2 of 2Next

Moderate

FDAJan 30, 2024Nationwide• Angiodynamics, Inc.

Angiodynamics, Inc.: MINI STICK MAX 5F X 10 CM STD .018 SS/SS ECHO 2.75" PG -U...

Moderate

FDAJan 30, 2024Nationwide• Angiodynamics, Inc.

Angiodynamics, Inc.: PulseSpray Infusion System devices including: PULSE SPRAY...

Rotating adaptor O-ring manufacturing defect impacting seal integrity which may lead to a leak during infusion of medication.

Moderate

FDADec 18, 2023Nationwide• Angiodynamics, Inc.

Angiodynamics, Inc.: NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indi...

Not programmed in accordance with specification. The programming affects the RFID function and does not allow the NanoKnife probes to be recognized by the NanoKnife generator resulting in a delay in procedure

Moderate

FDAMar 2, 2023Nationwide• Angiodynamics, Inc.

Angiodynamics, Inc.: Vortex MP Port Titanium Low Profile Implanted Port with 5...

Printed Instructions for Use (IFU) not shipped with device. The Instructions for Use contain the Warnings, Precautions, Contraindications, and Procedures for the Preparation, Implantation, and Post Operative Care of the implantable port, failure to follow the Instructions for Use may result in patient injury.

Moderate

FDASep 20, 2022Nationwide• Angiodynamics, Inc.

Angiodynamics, Inc.: VenaCure EVLT KIT WITH SPOTLIGHT OPS SHEATH 55CM Ref./ ...

OPS Fiber packaged within specific VenaCure EVLT Procedure Kits does not meet the required dimensional specification, may result in damage to the sheath, including separation or the inability to move the fiber within the sheath. A damaged sheath will necessitate removal from the patient, which may result in procedural delay and/or surgical intervention

Moderate

FDAAug 10, 2022Nationwide• Angiodynamics, Inc.