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All product recalls associated with Angiodynamics Inc. (Navilyst Medical Inc.).
Total Recalls
1000
Past Year
579
Class I (Serious)
91
Most Recent
Dec 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.
Snap lock connectors provided within implantable port kits may not meet dimensional specifications, and the catheter cannot be inserted into the snap lock connector prior to connection to the port chamber, resulting in a delay to the implantation procedure.
There is a potential performance issue as detected by an under-recovery of sample results during routine testing.
A portion of the lot was incorrectly packaged with a 12.5cm catheter instead of a 15cm catheter.