PlainRecalls

LeMaitre Vascular, Inc.

Compiled from official public sources by the publisher.

70 recalls on record · Latest: Mar 25, 2026

Subscribe to new LeMaitre Vascular, Inc. recalls (RSS)

Agency notice ledger

Federal filing book LeMaitre Vascular, Inc. MID-BOOK · SINGLE-AGENCY

#259 of 14,151 · 70 notices · 0.067% archive

  • BOOK 70 notices
  • RANK #259 of 14,151
  • SHARE 0.067% archive
  • AGENCY FDA Devices (70)
  • CAT medical devices
  • CATS 1 category
  • LATEST Mar 25, 2026
  • PHOTO Alcon Research LLC

Nearest notice-volume peer: Alcon Research LLC (0 notice gap)

LeMaitre Vascular, Inc. accounts for about 0.067% of the 104,423-notice archive on 70 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 LeMaitre Vascular, Inc. sits among 14,151 recalling firms

LeMaitre Vascular, Inc. ranks 259th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

LeMaitre Vascular, Inc. vs all firms by recall-notice count

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

70 259th of 14151 higher than 13,891 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

LeMaitre Vascular, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows LeMaitre Vascular, Inc. holds about 0.067% of archive notices alongside 70 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Low Mar 25, 2015

LeMaitre Vascular Tumescent Catheter Inversion (TCI) System. The TCI System is intended to provide a system to the removal of an incompetent greater saphenous vein. Catalog Number: 7210023, lot #61049252
FDA Devices Critical Jul 31, 2013

Albo Graft Knitted with Collagen, Bifurcate 16x08 Catalog Number: AMC1608 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Critical Jul 31, 2013

AlboGraft Knitted with Collagen, Straight 40x08 Catalog Number: AMC4008 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Critical Jul 31, 2013

AlboGraft Knitted with Collagen, Straight 60x08 Catalog Number: AMC6008 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Critical Jul 31, 2013

AlboGraft Woven with Collagen, Straight 15x30 Catalog Number: ATC1530 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Critical Jul 31, 2013

AlboGraft Woven with Collagen, Straight 30x18 Catalog Number: ATC3018 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Critical Jul 31, 2013

AlboGraft Knitted with Collagen, Straight 40x07 Catalog Number: AMC4007 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Critical Jul 31, 2013

AlboGraft Knitted with Collagen, Straight 60x06 Catalog Number: AMC6006 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Critical Jul 31, 2013

AlboGraft Knitted with Collagen, Bifurcate 20x10Catalog Number: AMC2010 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Critical Jul 31, 2013

AlboGraft Woven with Collagen, Straight 15x26 Catalog Number: ATC1526 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Critical Jul 31, 2013

AlboGraft Woven with Collagen, Straight 30x26 Catalog Number: ATC3026 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Critical Jul 31, 2013

AlboGraft Knitted with Collagen, Bifurcate 18x09 Catalog Number: AMC1809 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Critical Jul 31, 2013

AlboGraft Knitted with Collagen, Bifurcate 18x10 Catalog Number: AMC1810 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Critical Jul 31, 2013

AlboGraft Knitted with Collagen, Straight 60x07 Catalog Number: AMC6007 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Critical Jul 31, 2013

AlboGraft Woven with Collagen, Straight 30x16 Catalog Number: ATC3016 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Critical Jul 31, 2013

AlboGraft Woven with Collagen, Straight 30x24 Catalog Number: ATC3024 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Critical Jul 31, 2013

AlboGraft Knitted with Collagen, Straight 15x06 Catalog Number: AMC1506 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Critical Jul 31, 2013

AlboGraft Knitted with Collagen, Bifurcate 14x08 Catalog Number: AMC1408 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
FDA Devices Moderate Apr 10, 2013

Glow 'N Tell 20 cm Tape: 1100-00 (100 strips); 1100-50 (50 strips); 1100-20 (20 strips). Intended to be placed on the skin to assist during imaging procedures.
FDA Devices Moderate Apr 10, 2013

LeMaitre Stent Guide: 1102-00 (100 strips); 1102-50 (50 strips); 1102-20 (20 strips). Intended to be placed on the skin to assist during imaging procedures.

LeMaitre Vascular, Inc. 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 (70 here — heavy-book).

Alcon Research LLC 70 Chrysler,Dodge 70 Ethicon, Inc. 70 Kerry, Inc 70 Reliable Rexall-A Compounding Pharmacy 70

Similar medical devices volume

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

Alcon Research LLC 70 Ethicon, Inc. 70 Karl Storz Endoscopy 71 Zavation 71

Frequently Asked Questions

How many federal recall notices name LeMaitre Vascular, Inc.? ▼
PlainRecalls indexes 70 distinct federal recall events naming LeMaitre Vascular, 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 LeMaitre Vascular, Inc. sit among other recalling firms? ▼
LeMaitre Vascular, Inc. ranks #259 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 LeMaitre Vascular, Inc.'s notices? ▼
FDA Devices accounts for 70 of this firm's 70 indexed notices.
What product category dominates LeMaitre Vascular, Inc.'s filing book? ▼
Filings for LeMaitre Vascular, 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.
LeMaitre Vascular, Inc.: 70 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 LeMaitre Vascular, Inc.; individual notices remain authoritative on each linked recall page.

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