PlainRecalls

Maquet Cardiovascular, LLC

Compiled from official public sources by the editorial team.

251 recalls on record · Latest: Oct 1, 2025

Maquet Cardiovascular, LLC Recall Insight

Maquet Cardiovascular, LLC appears on 251 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.247% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Oct 1, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Jun 5, 2019 to May 13, 2020.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

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 …

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 o…

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 replaceme…

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 …

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 …

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 o…

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 …

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 …

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 …

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 o…

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 replaceme…

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

FDA Devices Moderate Jun 5, 2019

Maquet Getinge BEQ-TOP 38300 ADULT CPS QID Material:701055862R01

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.