company
Angiodynamics, Inc.
Jurisdiction: US
FDA Warning Letter timeline
V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 100CM 038 N…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 03…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 2 R/O Markers; ACCU…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACC…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 100CM 0…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 65CM 03…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: Soft -Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 038 N…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 65CM 0…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: Soft-Vu Angiographic Catheter, Cobra (1), Non-Braided; SOFT-VU CB1 4F X 100CM 0…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 65CM 038 N…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: Soft-Vu Angiographic Catheter, Straight Art, Non-Braided; SOFT-VU STR ART 4F X…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: AccuVu Angiographic Catheter, Straight Flush, Non-Braided, With 10 R/O Markers;…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: AccuVu Angiographic Catheter, Pigtail, Non-Braided, With 21 R/O Markers; ACCU-V…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: Soft-Vu Angiographic Catheter, Headhunter (1), Non-Braided; SOFT-VU HH1 4F X 10…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 035 NB…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 65CM 038 NB…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 03…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 100CM 035…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: Soft-Vu Angiographic Catheter, Sos Omni Selective (1), Non-Braided; SOFT-VU SO1…
- fda_recall · device_recall2026-04-29Angiodynamics, Inc. — Class II recall: Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 100CM…
Frequently asked questions
- How many FDA warning letters has Angiodynamics, Inc. received?
- Argus HQ has not recorded an FDA warning letter for Angiodynamics, Inc. in our current dataset.
- What FDA recalls has Angiodynamics, Inc. issued?
- Argus HQ has recorded 20 FDA recalls tied to Angiodynamics, Inc..
- Is Angiodynamics, Inc. FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 20 recalls, and 0 approval records for Angiodynamics, Inc.. Review the linked FDA source records directly before drawing a compliance conclusion.
Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.