Angiodynamics, Inc.: 52 recalls on record

Recalls filed with 1 agency: FDA (52).

First recall on record: June 5, 2013. Most recent: April 29, 2026.

Risk classification: Class II: 48 · Class III: 4

Most recent recalls

DateAgencyProduct
March 27, 2024FDAMINI STICK MAX 5F X 10 CM STIFF .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introd…Z-1341-2024
March 27, 2024FDAMINI STICK MAX 5F X 10 CM STD .018 SS/SS ECHO 1.6" PG- Used for the percutaneous introduc…Z-1345-2024
March 27, 2024FDAMINI STICK MAX 4F X 10 CM STIFF .018 SS/SS ECHO 2.75" PG-Used for the percutaneous introd…Z-1336-2024
March 27, 2024FDAMINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introdu…Z-1348-2024
March 27, 2024FDAMINI STICK MAX 4F X 10 CM STD .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduc…Z-1334-2024
March 27, 2024FDAMINI STICK MAX 4F X 10 CM STIFF .018 NI/TU NON-ECHO 2.75" PG- Used for the percutaneous …Z-1342-2024
March 27, 2024FDAMINI STICK MAX 5F X 10 CM STD .018 SS/SS ECHO 2.75" PG -Used for the percutaneous introdu…Z-1338-2024
March 27, 2024FDAMINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG-Used for the percutaneous intr…Z-1344-2024
March 27, 2024FDAMINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introdu…Z-1346-2024
March 27, 2024FDAMINI STICK MAX 5F X 15 CM STIFF .018 NI/TU NON-ECHO 2.75" PG-Used for the percutaneous i…Z-1347-2024
February 14, 2024FDAPulseSpray Infusion System devices including: PULSE SPRAY 5F/135/20, UPN: H787125004045, …Z-1010-2024
September 15, 2021FDASolero Generator US PG, Item No. H78712740000US0, Catalog No. 12740000USZ-2437-2021
June 24, 2020FDABioFlo Midline Convenience Kits - Product Usage: These introducers are used for the percu…Z-2396-2020
June 24, 2020FDABioFlo PICC and Xcela PICC Maximal Barrier Nursing Kits - Product Usage: are indicated fo…Z-2398-2020
December 28, 2016FDAANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Stiffened Mi…Z-0776-2017
December 28, 2016FDAANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Stiffened Mi…Z-0773-2017
December 28, 2016FDAANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Mi…Z-0775-2017
December 28, 2016FDAANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Mi…Z-0772-2017
December 28, 2016FDAANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Mi…Z-0777-2017
April 13, 2016FDANAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT, REF Catalog No. 601319810, UPN …Z-1346-2016
April 13, 2016FDANAMIC CONVENIENCE KIT SELF REGIONAL HEALTHCARE PV LEG PACK, REF Catalog No. 651919311, UP…Z-1343-2016
August 27, 2014FDAUni*Fuse INFUSION SYSTEM WITH COOPER WIRE, 5F x 90 cm x 10 cm Infusion Pattern, Catalog N…Z-2260-2014
August 27, 2014FDAUni*Fuse INFUSION SYSTEM WITH COOPER WIRE, 5F x 90 cm x 30 cm Infusion Pattern, Catalog N…Z-2261-2014
August 27, 2014FDAUni*Fuse INFUSION SYSTEM WITH COOPER WIRE, 5F x 90 cm x 40 cm Infusion Pattern, Catalog N…Z-2262-2014
July 17, 2013FDAAngioDynamics RITA Main Cable, 9 Pin to 14 Pin, REF 700-101892. RITA Main Cables are indi…Z-1675-2013

Questions about this company

How many recalls does Angiodynamics, Inc. have?
Recalert has 52 U.S. recalls on record for Angiodynamics, Inc., published between June 5, 2013 and April 29, 2026.
Which agencies have handled Angiodynamics, Inc. recalls?
Angiodynamics, Inc. appears as the recalling firm in recalls from: FDA (52).

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