PlainRecalls

Angiodynamics Inc. (Navilyst Medical Inc.)

Compiled from official public sources by the publisher.

78 recalls on record · Latest: Oct 6, 2021

Subscribe to new Angiodynamics Inc. recalls (RSS)

Agency notice ledger

Federal filing book Angiodynamics Inc. MID-BOOK · SINGLE-AGENCY

#231 of 14,151 · 78 notices · 0.075% archive

  • BOOK 78 notices
  • RANK #231 of 14,151
  • SHARE 0.075% archive
  • AGENCY FDA Devices (78)
  • CAT medical devices
  • CATS 1 category
  • LATEST Oct 6, 2021
  • PHOTO Draeger Medical, Inc.

Nearest notice-volume peer: Draeger Medical, Inc. (0 notice gap)

Angiodynamics Inc. (Navilyst Medical Inc.) accounts for about 0.075% of the 104,423-notice archive on 78 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Angiodynamics Inc. sits among 14,151 recalling firms

Angiodynamics Inc. (Navilyst Medical Inc.) ranks 231st of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Angiodynamics Inc. vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

78 231st of 14151 higher than 13,917 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Angiodynamics Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Angiodynamics Inc. (Navilyst Medical Inc.) holds about 0.075% of archive notices alongside 78 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Oct 6, 2021

Xcela PICC with PASV Valve Technology/Kit 5 F-55cm; (Maximum Flow Rate 3.5 mL/Sec)-indicated for short or long-term peripheral access to the central venous system for intravenous therapy, including but not limited to, the administration of fluids, medications, and nutrients; the sampling of blood; and for power injection of contrast media. Catalog Number: 60M701995
FDA Devices Moderate Apr 28, 2021

AngioDynamics Safe Sheath Ultralite - Vascular Introducer/Catheter Introducer Catalogue #: VI10 - Product Usage: For the introduction of various types of pacing leads and catheters.
FDA Devices Moderate Apr 28, 2021

Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI, CT96STSA-VI - Product Usage: indicated for any patient requiring repeated access of the vascular system, for delivery of medications, nutritional supplementation, fluids, blood, blood products, and sampling of blood and power injection of contrast media for imaging.
FDA Devices Moderate Nov 27, 2019

BIOFLO 8F SINGLE TITANIUM NON- FILLED; VALVED, UPN H965440250, Cat. No. 44-025 - Product Usage: Long-term access to the central venous system for administration of fluids including but not limited to hydration fluids, chemotherapy, analgesics, nutritional therapy and blood products. The device is also indicated for blood specimen withdrawal.
FDA Devices Moderate Nov 27, 2019

BIOFLO 8F SINGLE PLASTIC FILLED; VALVED, UPN H965440220, Cat. No. 44-022
FDA Devices Moderate Nov 27, 2019

BIOFLO 8F SINGLE PLASTIC FILLED; NON-VALVED, UPN H965440140, Cat. No. 44-014 - Product Usage: Long-term access to the central venous system for administration of fluids including but not limited to hydration fluids, chemotherapy, analgesics, nutritional therapy and blood products. The device is also indicated for blood specimen withdrawal.
FDA Devices Moderate Nov 27, 2019

XCELA, 8F SINGLE PLASTIC PORT FILLED, VALVED, UPN H965440400, Cat. No. 44-040 - Product Usage: Long-term access to the central venous system for administration of fluids including but not limited to hydration fluids, chemotherapy, analgesics, nutritional therapy and blood products. The device is also indicated for blood specimen withdrawal.
FDA Devices Moderate Nov 27, 2019

BIOFLO 8F SINGLE PLASTIC NON-FILLED; VALVED, UPN H965440210, Cat. No. 44-021 - Product Usage: Long-term access to the central venous system for administration of fluids including but not limited to hydration fluids, chemotherapy, analgesics, nutritional therapy and blood products. The device is also indicated for blood specimen withdrawal.
FDA Devices Moderate Nov 27, 2019

Starburst Talon Semi-Flex Electrosurgical Device, Part Number H7877001028451 incorrectly labelled as Starburst MRI Semi-Flex Electrosurgical Device, Part Number H7877001026151
FDA Devices Moderate Jun 12, 2019

AngioDynamics Solero Microwave Tissue Ablation (MTA) System: Solero Generator PG (1) Catalog Number:12740000 UPN: H78712740000 (2) Solero Generator US PG Catalog Number: 12740000US UPN: H78712740000US0 (3) Solero Generator Service Loaner PG Catalog No: 12740000L UPN: H78712740000L0 (4) Solero Generator Service Loaner US PG Catalog Number: 12740000USL UPN: H78712740000USL0
FDA Devices Moderate Jun 12, 2019

AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1) Solero Applicator 14cm PG Catalog Number: 700106001 UPN:H7877001060010; (2)Solero Applicator 14cm PG US Catalog Number:700106001US UPN: H787700106001US0 Product Usage: The Solero Microwave Tissue Ablation (MTA) System and accessories are indicated for the ablation of soft tissue during open procedures. The Solero MTA System is not intended for cardiac use.
FDA Devices Moderate Jun 12, 2019

AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1)Solero Applicator 29cm PG Catalog Number:700106003 UPN: H7877001060030 (2)Solero Applicator 29cm PG US Catalog Number:700106003US UPN:H787700106003US0 Product Usage: The Solero Microwave Tissue Ablation (MTA) System and accessories are indicated for the ablation of soft tissue during open procedures. The Solero MTA System is not intended for cardiac use.
FDA Devices Moderate Jun 12, 2019

AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1) Solero Generator Refurbished PG Catalog Number: 12740000D UPN: H78712740000D0 (2) Solero Generator Refurbished US PG Catalog Number: 12740000USD ;UPN: H78712740000USD0
FDA Devices Moderate Jun 12, 2019

AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1)Solero Applicator 19cm PG Catalog Number: 700106002 UPN: H7877001060020 (2)Solero Applicator 19cm PG US Catalog Number:700106002US UPN: H787700106002US0 Product Usage: The Solero Microwave Tissue Ablation (MTA) System and accessories are indicated for the ablation of soft tissue during open procedures. The Solero MTA System is not intended for cardiac use.
FDA Devices Moderate Dec 19, 2018

Xcela Power Injectable PICC with PASV (XCELA PASV 4F SL 55CM Catheter Kit CE PG), Cat no. 55-711
FDA Devices Moderate Dec 19, 2018

BioFlo PICC with ENDEXO and PASV, ( RS 5F DL BIOFLO PASV - MEMORIAL HOSPITAL SYSTEM (LTP) PG) Cat. no. 60M183481
FDA Devices Moderate Oct 17, 2018

BioFlo Port with ENDEXO and PASV Technology-AngioDynamics BIOFLO 8F SINGLE PLASTIC NON-FILLED; VALVED PG UPN: H965440210 Catalog Number: 44-021 Box of 1 Port - Product Usage - Long-term access to the central venous system for administration of fluids including but not limited to hydration fluids, chemotherapy, analgesics, nutritional therapy and blood products. The device is also indicated for blood specimen withdrawal.
FDA Devices Moderate Jun 20, 2018

CAN 5F SINGLE XCELA PICC, Catalog Number 60M701531
FDA Devices Moderate Jun 20, 2018

5F DL BIOFLO PASV, Catalog Number 60M141006
FDA Devices Moderate Jun 20, 2018

RS 5F DL BIOFLO PASV, Catalog Number 60M132324
FDA Devices Moderate Jun 20, 2018

BioFlo Midline 5F DL-20cm MST-45 Kit w/ Two Nitinol Guidewires PG, Catalog Number 46-810
FDA Devices Moderate Jun 20, 2018

RS TANDEM 5F DL XPP, Catalog Number 60M019881
FDA Devices Moderate Jun 20, 2018

5F DL BIOFLO PICC, Catalog Number 60M180592
FDA Devices Moderate Jun 20, 2018

BioFlo PICC (NV) 5FSL-55cm Maximal Barrier Nursing Kit w/ 70cm Nitinol Wire PG, Catalog Number 75-032
FDA Devices Moderate Jun 20, 2018

CAN 5F DUAL XCELA PICC, Catalog Number 60M701532
FDA Devices Moderate Jun 20, 2018

RS TANDEM 5F DL XCELA PICC PASV, Catalog Number 60M181582
FDA Devices Moderate Jun 20, 2018

RS 5F DL BIOFLO PASV, Catalog Number 60M150373
FDA Devices Moderate Jun 20, 2018

Xcela 5FDL-55cm Maximal Barrier Nursing Kit PG, Catalog Number 75-003
FDA Devices Moderate Jun 20, 2018

Bio-Stable 5F DL-55CM IR-145 Kit Non-Valved PG, Catalog Number 45-872
FDA Devices Moderate Jun 20, 2018

RS 5F DL BIOFLO PASV, Catalog Number 60M181578
FDA Devices Moderate Jun 20, 2018

RS 5F DL BIOFLO PICC, Catalog Number 60M071831
FDA Devices Moderate Jun 20, 2018

BioFlo Midline 5F DL-20cm Max Sterile Barrier Drape Kit w/ Two Nitinol Guidewire PG, Catalog Number 46-490
FDA Devices Moderate Jun 20, 2018

Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved PG, Catalog Number 45-871
FDA Devices Moderate Jun 20, 2018

XCELA PASV 5F SL 55CM IR-145 Nitinol Wire KIT PG, Catalog Number 25-124
FDA Devices Moderate Jun 20, 2018

Bio-Stable 5F SL-55CM IR-145 Kit Valved with Nitinol GW PG, Catalog Number 45-882
FDA Devices Moderate Jun 20, 2018

Bio-Stable 5F DL-55CM IR-145 Kit Non-Valved with Nitinol GW PG, Catalog Number 45-887
FDA Devices Moderate Jun 20, 2018

RS 5F DL XPP KIT, Catalog Number 60M183104
FDA Devices Moderate Jun 20, 2018

Bio-Stable 5F SL-55CM MST-70 Kit Valved with Nitinol Guidewire PG, Catalog Number 45-892
FDA Devices Moderate Jun 20, 2018

CAN 5F DL BIOFLO PASV PICC NURSING TRAY, Catalog Number 60M700936
FDA Devices Moderate Jun 20, 2018

RS 5F DL BIOFLO PASV, Catalog Number 60M183481
FDA Devices Moderate Jun 20, 2018

RS - TANDEM 5F DL BIOFLO MIDLINE, Catalog Number 60M035472
FDA Devices Moderate Jun 20, 2018

RS TANDEM 5F DL BIOFLO PASV, Catalog Number 60M232242
FDA Devices Moderate Jun 20, 2018

Bio-Stable 5F SL-55CM IR-145 Kit Valved PG, Catalog Number 45-818
FDA Devices Moderate Jun 20, 2018

RS 5F DL XCELA PICC, Catalog Number 60M122272
FDA Devices Moderate Jun 20, 2018

BioFlo PICC (Valved) 5FDL-55cm Maximal Barrier Nursing Kit PG, Catalog Number 75-019
FDA Devices Moderate Jun 20, 2018

TANDEM 5F DL BIOFLO PASV, Catalog Number 60M140567
FDA Devices Moderate Jun 20, 2018

Bio-Stable 5F SL-55CM IR-145 Kit Non-Valved with Nitinol GW PG, Catalog Number 45-886
FDA Devices Moderate Jun 20, 2018

RS TANDEM 5F DL BIOFLO PASV, Catalog Number 60M120196
FDA Devices Moderate Jun 20, 2018

BioFlo PICC (Valved) 5FDL-55cm Maximal Barrier Nursing Kit w/70cm Nitinol Wire PG, Catalog Number 75-038
FDA Devices Moderate Jun 20, 2018

RS 5F DL XPP, Catalog Number 60M030393

Angiodynamics Inc. carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Draeger Medical, Inc. 78 Wright Medical Technology, Inc. 78 Abiomed, Inc. 79 Philips Medical Systems Nederlands 79

Frequently Asked Questions

How many federal recall notices name Angiodynamics Inc.? ▼
PlainRecalls indexes 78 distinct federal recall events naming Angiodynamics Inc. (Navilyst Medical Inc.), aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Angiodynamics Inc. sit among other recalling firms? ▼
Angiodynamics Inc. (Navilyst Medical Inc.) ranks #231 of 14,151 by distinct recall-event count among 14,151 firms in this archive (98th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Angiodynamics Inc.'s notices? ▼
FDA Devices accounts for 78 of this firm's 78 indexed notices.
What product category dominates Angiodynamics Inc.'s filing book? ▼
Filings for Angiodynamics Inc. (Navilyst Medical Inc.) span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Angiodynamics Inc. (Navilyst Medical Inc.): 78 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Angiodynamics Inc. (Navilyst Medical Inc.); individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026