Maquet Cardiovascular, LLC
252 recalls on record · Latest: Jul 22, 2026
Subscribe to new Maquet Cardiovascular, LLC recalls (RSS)
Agency notice ledger
Federal filing book Maquet Cardiovascular, LLC HEAVY-BOOK · SINGLE-AGENCY
#52 of 14,151 · 252 notices · 0.241% archive
- BOOK 252 notices
- RANK #52 of 14,151
- SHARE 0.241% archive
- AGENCY FDA Devices (252)
- CAT medical devices
- CATS 1 category
- LATEST Jul 22, 2026
- PHOTO Nissan
Nearest notice-volume peer: Nissan (1 notice gap)
Maquet Cardiovascular, LLC accounts for about 0.241% of the 104,423-notice archive on 252 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 →
Maquet Cardiovascular, LLC's standing among 14,151 recalling firms
Maquet Cardiovascular, LLC ranks 52nd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.
Maquet Cardiovascular, LLC vs all firms by recall-notice count
Where this firm's archive sits among every tracked recalling manufacturer
252 52nd of 14151 higher than 14,099 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
Maquet Cardiovascular, LLC in the notice-volume neighbourhood
Distinct federal recall events among this firm and nearest nationwide peers
- Hospira Inc.
Hospira Inc.
257 notices
- Intuitive Sur…
Intuitive Surgical, Inc.
257 notices
- Biomet, Inc.
Biomet, Inc.
255 notices
- Nissan
Nissan
253 notices
- Maquet Cardio… (this)
Maquet Cardiovascular, LLC
252 notices
- Volvo
Volvo
248 notices
What this shows Maquet Cardiovascular, LLC holds about 0.241% of archive notices alongside 252 distinct filings.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 4 Branch, Product Code: M00202175734P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175828P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175926P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
Hemashield Gold Knitted Microvel Double Velour Vascular Graft-Axillo-bifemoral, Product Code: M002020955880 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Thoracoabdominal, Product Code: M00202175426T0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175824P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175922P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch, Product Code: M00202175728AP0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175830P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175820P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch, Product Code: M00202175914P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
Hemashield Gold Knitted Microvel Double Velour Vascular Graft-Axillo-bifemoral, Product Code: M002020955010 - Product Usage: For use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 5502 ECC Pack Material:701051791R01
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 21502# Med City Childr Material: 701050060
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BO-TOP 15200 OR PACK HMO & RF Material:701050647R01
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 22701 Material: 701050790
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 41201 ECC 3/8 PUMP PAC Material: 701064867
FDA Devices Moderate Jun 5, 2019
Maquet Getinge- BO-TOP 13901 Rapid Response Universal Pk Material: 701054874R01
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-T 3502 LVAD 1/4" Material: 701068168
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-T 37305 1/4+3/8 TABLE LINE Material: 701067577
FDA Devices Moderate Jun 5, 2019
Maquet Getinge- (1)Material: 701065765R01 BO-TOP 36504 Adult ECC Pack (2)Material: 701065765R02 BO-TOP 36504 Adult ECC Pack
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 24202 ADULT ECC Material:701054295
FDA Devices Moderate Jun 5, 2019
Maquet Getinge- BEQ-TOP 32200 ECC Pack Material: 701053319R01
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 5208 ECC SET CARDIAC Material: 701067350
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 35503 SGD Pack Material:701068797R01
FDA Devices Moderate Jun 5, 2019
Maquet Getinge BO-TOP 48400 OR PACK Material: 701064327R01
FDA Devices Moderate Jun 5, 2019
Maquet Getinge- BEQ-TOP 28901 MCV INFANT ECC Material:701056771R01
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-T 48003 Rotaflow ONLY Support Pack Material:709000490
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-T 25501 3/8" Better Bladder Pack Material: 709000370
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 44701 PEDIATRIC ECC Material: 701064825
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 5909 1/4 PACK W QPID Material: 701064992
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-T 8506 Transport Pack Material: 709000146
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 33501 1/4" ECC PACK Material: 701053754
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 38900 ECC PACK Material: 701056368
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 8013 ECC QUADROX iD Pack RF32 Material: 701047962
FDA Devices Moderate Jun 5, 2019
Maquet Getinge- BEQ-TOP 37200 E-Circuit Bioline Heparin Material: 701055388R01
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BO-TOP 28903 Adult ECC Pack Material: 709000093
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-T 8805 ECC PACK Material: 701053361
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 33704 ECC 1/4" PACK Material: 701054150
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-T 8030 4 in High Flow Pigtail Material: 709000366
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 27901 SMALL PATIENT CI Material:701052287
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-T 51501 Ochsner ECC Pack Material:709000113
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-T 3502 LVAD 1/4" Material: 701068168R01
FDA Devices Moderate Jun 5, 2019
Maquet Getinge- (1) Material: 701067350R01 BEQ-TOP 5208 ECC Small-Cardiac (2) material: 701067350R02 BEQ-TOP 5208 ECC Small-Cardiac
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 9004 1/4 Custom Pk w/RF32 & HMOD Material: 701054451R01
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 33700 ECC 3/8" PACK Material: 701053845
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-T 5914 TCH ¿ Inch Change Kit Material: 709000334
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 21502 ECC Quadrox iD w/RF 3/8" Material:701050060R01
FDA Devices Moderate Jun 5, 2019
Maquet Getinge- BEQ-T 9411 Lurie Children's 1/4 ADAPT Material:709000485R01
FDA Devices Moderate Jun 5, 2019
Maquet Getinge-BEQ-TOP 26402 ECC PACK Material: 701062310
Maquet Cardiovascular, LLC 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 (252 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 Maquet Cardiovascular, LLC? ▼
PlainRecalls indexes 252 distinct federal recall events naming Maquet Cardiovascular, LLC, 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 Maquet Cardiovascular, LLC sit among other recalling firms? ▼
Maquet Cardiovascular, LLC ranks #52 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 Maquet Cardiovascular, LLC's notices? ▼
FDA Devices accounts for 252 of this firm's 252 indexed notices.
What product category dominates Maquet Cardiovascular, LLC's filing book? ▼
Filings for Maquet Cardiovascular, LLC 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.
Maquet Cardiovascular, LLC: 252 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 Maquet Cardiovascular, LLC; individual notices remain authoritative on each linked recall page.
Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026