PlainRecalls

Maquet Cardiovascular, LLC

177 recalls on record · Latest: Oct 1, 2025

Maquet Cardiovascular, LLC Recall Insight

Maquet Cardiovascular, LLC appears on 177 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.211% 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 27 entries, severity tagging shows 0 critical, 27 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 27 of 27 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 (27). The date window on this page runs from Jan 16, 2013 to Jun 5, 2019.

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 Jun 5, 2019

Maquet Getinge-BEQ-TOP 5900 3/8 Quadrox iD Pack w/BB Material: 701050228

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BO-TOP 20705 SMALL PATIENT 1/4 Material: 701053486

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BEQ-T 8068 1/4" WITH BRIDGE Material: 701066883

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BO-T 2303 Small Adult Cardiac Surgery Material:709000004

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BEQ-TOP 49103 ECC Pack 0 No Bladder Material: 709000058

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BEQ-TOP 4901 Material: 701050839

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-T 22706 SAMPLE MANIFOLD Material:701054912

FDA Devices Moderate Jun 5, 2019

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

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BEQ-TOP 8207 1/4" ECC PACK Material: 701068395

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BO-T 46201 Small Pediatric Cardiac Surge Material: 709000133

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BEQ-T 36507 Accessory Pk Mercy Material: 709000390

FDA Devices Moderate Jun 5, 2019

Maquet Getinge- BEQ-TOP 46700 ADULT ECC PACK Material:701065833R01

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BEQ-TOP 28601 NEONATE ECC QPiD Material: 701051935R01

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BEQ-TOP 33500 3/8" ECC PACK Material: 701053752

FDA Devices Moderate Jun 5, 2019

Maquet Getinge- BEQ-TOP 41201 ECC 3/8 Pump Pack Wake For Material: 701064867R01

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BEQ-TOP 31604 CHKD 1/4" ECC Material: 709000518

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BEQ-T-22800 Material: 701049506

FDA Devices Moderate Jun 5, 2019

Maquet Getinge- BEQ-T 53500 Evanston Rotaflow Pack Material:709000215R01

FDA Devices Moderate Jun 5, 2019

Maquet Getinge- BEQ-TOP 54500 BSW-McLANE 3/8 Quadrox iD Material:709000496R01

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BO-TOP 20700 SMALL PATIENT 3/8 Material: 701050966

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BEQ-TOP 24500 ADULT ECC Material: 701050253

FDA Devices Moderate Mar 13, 2019

AXIUS Blower Mister Product Code/REF Number: CB-1000 The Axius Blower Mister is intended to clear an anastomotic site for improved visibility

FDA Devices Moderate Mar 22, 2017

VASOVIEW HEMOPRO VH-3500 ENDOSCOPIC VESSEL HARVESTING SYSTEM Product Usage: The VASOVIEW HEMOPRO VH-3500 is designed for use in conjunction with…

FDA Devices Moderate Nov 5, 2014

Acrobat V Vacuum Off-Pump System OM-9100S Acrobat SUV Vacuum Off-Pump System OM-9000S Axius Xpose 3 Access Device XP-3000 XPOSE 4 Access D…

FDA Devices Moderate Oct 9, 2013

Ultima OPCAB System, Sterile, Rx Only, Product Usage: Intended for use during performance of minimally invasive cardiac surgery through a sterno…

FDA Devices Moderate Apr 24, 2013

MAQUET CARDIOHELP Support System: CARDIOHELP-I Software (up to version 3.3.0.0) Product Usage: The Cardiohelp System is a blood oxygenation and …

FDA Devices Moderate Jan 16, 2013

CARDIOSAVE Intra-Aortic Balloon Pump An electromechanical system used to inflate and deflate intra-aortic balloons. It provide temporary support t…

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Data Sources

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