Medtronic Vascular, Inc. recalls
Every recall we track for Medtronic Vascular, Inc. — 11 in all, from 2017–2022 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Medtronic Vascular, Inc. peaked in 2021 (8); 11 since 2017.
All FDA recall records for Medtronic Vascular, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 1 | 0 | 1 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 3 | 3 | 2 | 8 |
| 2022 | 0 | 0 | 1 | 1 | 2 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Medtronic Vascular, Inc. recalls
What to do if you have a recalled Medtronic Vascular, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Medtronic Vascular, Inc. recalls
7 shown- Lower riskMedical device
Medtronic Vascular, Inc. recalls Medtronic IN.PACT AV, Paclitaxel-coated PTA Balloon Catheter, REF: IAV06008008P, Sterile EO, Rx Only
Medtronic recalls Paclitaxel-coated PTA balloon catheters with packaging that may lose sterility, risking infection during procedures. Affected units include specific lot numbers and model codes.
MedtronicMar 23, 2022 - Use cautionMedical device
Medtronic Vascular, Inc. recalls Endurant, Endurant II and Endurant IIs Stent Graft System: Medtronic Endurant Stent Graft System Model/REF
Medtronic recalls Endurant, Endurant II, and Endurant IIs stent graft systems with specific batch numbers that may detach during implant, requiring removal or leaving behind in patients.
MedtronicDec 21, 2021 - UnratedMedical device
Medtronic Vascular, Inc. recalls Endurant II Stent Graft System REF/Description: ETBF2513C145EE STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2820C166EE
Medtronic recalls Endurant II Stent Graft Systems with specific model numbers due to risk of spindle detaching during deployment, which could cause complications. Affected units include ETBF2513C145EE and other variants listed in the recall.
MedtronicOct 15, 2021 - Use cautionMedical device
Medtronic Vascular, Inc. recalls Endurant II/Endurant IIs Stent Graft System: Medtronic Endurant II Stent Graft System REF ETUF3214C102EE,
Medtronic recalls Endurant II stent graft systems with specific model numbers due to risk of radiopaque marker detaching during deployment, potentially causing complications.
MedtronicJun 7, 2021 - Lower riskMedical device
Medtronic Vascular, Inc. recalls Endurant II/IIs Stent Graft System: STENT GRAFT ETBF3216C145E ENDUR II BIF. For treatment of vascular aneurysms.
Medtronic recalls Endurant II stent grafts with incorrect stentstop assembly (18fr) that could cause device malfunction during vascular aneurysm treatment.
MedtronicApr 28, 2021 - Lower riskMedical device
Medtronic Vascular, Inc. recalls Valiant Navion Thoracic Stent Graft System. For endovascular repair of lesions in the descending thoracic aorta (DTA).
Medtronic Vascular recalls Valiant Navion Thoracic Stent Graft System (models VNMC2020C94TE, VNMC2020C94TJ, etc.) for endoleaks, stent fractures, and stent ring enlargement. Affected patients should contact Medtronic for evaluation.
TrsmimaFeb 12, 2021 - Lower riskMedical device
Medtronic Vascular, Inc. recalls Medtronic Aptus Heli-FX Thoracic EndoAnchor System Heli-FX Guide 42 mm, REF HG-18-90-42, STERILE EO, Rx Only The
Medtronic recalls specific Heli-FX Thoracic EndoAnchor System guides due to mismatched deflection length labels on packaging versus actual product. This may affect medical procedures requiring precise catheter handling.
MedtronicSep 13, 2017
Medtronic Vascular, Inc. recall questions
How many recalls has Medtronic Vascular, Inc. had?
11 recalls from Medtronic Vascular, Inc. are on record with U.S. safety agencies, from 2017–2022.
What is the most recent Medtronic Vascular, Inc. recall?
Medtronic Vascular, Inc. recalls Medtronic IN.PACT AV, Paclitaxel-coated PTA Balloon Catheter, REF: IAV06008008P, Sterile EO, Rx Only, dated Mar 23, 2022. Every Medtronic Vascular, Inc. recall is listed on this page, newest first.
Why are Medtronic Vascular, Inc. products recalled?
The most common reasons on record: Packaging for Balloon Catheters may be damaged resulting in loss of sterility. (2).
What should I do if I have a recalled Medtronic Vascular, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Medtronic Vascular, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.