Medtronic Vascular
211 recalls on record · Latest: Jun 23, 2021
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Agency notice ledger
Federal filing book Medtronic Vascular HEAVY-BOOK · SINGLE-AGENCY
#65 of 14,151 · 211 notices · 0.202% archive
- BOOK 211 notices
- RANK #65 of 14,151
- SHARE 0.202% archive
- AGENCY FDA Devices (211)
- CAT medical devices
- CATS 1 category
- LATEST Jun 23, 2021
- PHOTO Exactech, Inc.
Nearest notice-volume peer: Exactech, Inc. (0 notice gap)
Medtronic Vascular accounts for about 0.202% of the 104,423-notice archive on 211 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 Medtronic Vascular sits among 14,151 recalling firms
Medtronic Vascular ranks 65th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.
Medtronic Vascular vs all firms by recall-notice count
Where this firm's archive sits among every tracked recalling manufacturer
211 65th of 14151 higher than 14,086 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
Medtronic Vascular in the notice-volume neighbourhood
Distinct federal recall events among this firm and nearest nationwide peers
- Integra LifeS…
Integra LifeSciences Corp.
217 notices
- Medtronic Vas… (this)
Medtronic Vascular
211 notices
- Exactech, Inc.
Exactech, Inc.
211 notices
- Philips Medic…
Philips Medical Systems Nederland B.v.
209 notices
- Volkswagen
Volkswagen
207 notices
- Teleflex Medi…
Teleflex Medical
204 notices
What this shows Medtronic Vascular holds about 0.202% of archive notices alongside 211 distinct filings.
FDA Devices Critical Jun 23, 2021
Angiographic Guidewire Component: Model Number: 107042, 107044, 107447, 110003, 110004, The angiographic guidewire components associated with this recall are manufactured with a requirement that further downstream processing (sterilization) is required. Indications for use for these components are not defined as they are not intended for final use.
FDA Devices Moderate Mar 17, 2021
Medtronic 6F Launcher Guide Catheter 100 cm EBU 3.0 Model Number: LA6EBU30
FDA Devices Moderate Mar 17, 2021
Medtronic 6F Launcher Guide Catheter 100cm EBU 3.75 Model Number: LA6EBU375
FDA Devices Moderate Mar 17, 2021
Medtronic 6F Launcher Guide Catheter 100 cm JR 4.0 Model Number: LA6JR40
FDA Devices Moderate Mar 17, 2021
Medtronic 6F Launcher Guide Catheter 100 cmJL 3.5 Model Number: LA6JL35
FDA Devices Critical Oct 28, 2020
Rashkind Balloon Septostomy Catheter, 6F, Recess Balloon, Closed end, 50 cm, Pediatric, Single Lumen Product number: 008764 GTIN: 00613994760289 The Rashkind balloon septostomy catheters are designed for creating an atrial septal defect or enlarging an existing atrial septal defect as a treatment option for patients with a Cyanotic Congenital heart defect. Cyanotic congenital heart defects are rare conditions that are associated with high morbidity and mortality.
FDA Devices Critical Oct 28, 2020
Rashkind Balloon Septostomy Catheter, 4F, Closed end, 50 cm, Pediatric, Single Lumen Product number: 007161 GTIN: 00613994760272 The Rashkind balloon septostomy catheters are designed for creating an atrial septal defect or enlarging an existing atrial septal defect as a treatment option for patients with a Cyanotic Congenital heart defect. Cyanotic congenital heart defects are rare conditions that are associated with high morbidity and mortality.
FDA Devices Critical Oct 28, 2020
Rashkind Balloon Septostomy Catheter, 5F, Closed end, 50 cm, Pediatric, Single Lumen Product number: 007160 GTIN: 00613994760265 The Rashkind balloon septostomy catheters are designed for creating an atrial septal defect or enlarging an existing atrial septal defect as a treatment option for patients with a Cyanotic Congenital heart defect. Cyanotic congenital heart defects are rare conditions that are associated with high morbidity and mortality.
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F AL1.0, .070", REF SA6AL10. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F JL3.0 SH, .070", REF SA6JL30SH. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F, 3DRC 100CM .070", REF SA63DRC. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F ERAD RIGHT SHORT TIP, .070", REF SA6ERADRST. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F SL4.5, .070", REF SA6SL45. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F AL2.0, .070", REF SA6AL20. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F LCB 90CM, .070", REF SA6LCBD. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F 110CM AL20, REF SA6AL20A. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F SL5.0, .070", REF SA6SL50. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F CHAMP2.0 SH, .070", REF SA6CHAMP20SH. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F AL.75, .070", REF SA6AL75. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F EBU4.0 SH, .070", REF SA6EBU40SH. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F LARA, .070", REF SA6LARA. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F SL4.0, .070", REF SA6SL40. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F, RDND1 55CM .070", REF SA6RDND1K. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F CHAMP1.0 SH, .070", REF SA6CHAMP10SH. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F SAL.75, .070", REF SA6SAL75. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F EBU3.5 SH, .070", REF SA6EBU35SH. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F, CHAMP2.0, 55CM.070", REF SA6CHAMP20K. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F AL3.0, .070", REF SA6AL30. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F SR3.5 SH, .070" REF SA6SR35SH. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F RBU4.5, .070", REF SA6RBU45. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F SCR3.5 SH, .070", REF SA6SCR35SH. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F MAC5.0, .070", REF SA6MAC50. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F CHAMP3.5, .070", REF SA6CHAMP35. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F EBU4.5, .070", REF SA6EBU45. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F ERAD LEFT, .070", REF SA6ERADL. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F ALR1-2 SH, .070", REF SA6ALR12SH. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F SAL1.5, .070", REF SA6SAL15. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F EL GAMAL SH, .070", REF SA6ELGAMALSH. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F M RADIAL, .070", REF SA6MRADIAL. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F, PK1, 47CM, 070", REF SA6PK1W. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F MAC4.0, .070", REF SA6MAC40. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F JL4.5 SH, .070", REF SA6JL45SH. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F, CHAMP0.5, 100CM.070", REF SA6CHAMP05. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F RCB, .070", REF SA6RCB. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F ECR4.0 SH, .070", REF SA6ECR40SH. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F, MB1, 90CM, 070", REF SA6MB1D. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F CHAMP2.0, .070", REF SA6CHAMP20. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F CHAMP3.0, .070", REF SA6CHAMP30. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F ERAD LEFT, LONG TIP, .070", REF SA6ERADLLT. for cardiovascular use
FDA Devices Critical Oct 9, 2019
SHERPA NX ACTIVE GUIDING CATHETER, 6F EBU4.5 SH, .070", REF SA6EBU45SH. for cardiovascular use
Medtronic Vascular carries an outsized archive share
Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.
Similar recall count
Nearest multi-notice firms by distinct-event totals (211 here — heavy-book).
Similar medical devices volume
Nearest multi-notice firms in the same narrow category lane.
Frequently Asked Questions
How many federal recall notices name Medtronic Vascular? ▼
PlainRecalls indexes 211 distinct federal recall events naming Medtronic Vascular, 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 Medtronic Vascular sit among other recalling firms? ▼
Medtronic Vascular ranks #65 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Medtronic Vascular's notices? ▼
FDA Devices accounts for 211 of this firm's 211 indexed notices.
What product category dominates Medtronic Vascular's filing book? ▼
Filings for Medtronic Vascular 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.
Medtronic Vascular: 211 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 Medtronic Vascular; individual notices remain authoritative on each linked recall page.
Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026