PlainRecalls

Draeger Medical, Inc.

58 recalls on record · Latest: Dec 25, 2024

Draeger Medical, Inc. Recall Insight

Draeger Medical, Inc. appears on 58 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.069% 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 Dec 25, 2024, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 34 critical, 16 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 Aug 3, 2016 to Dec 25, 2024.

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 Critical Dec 25, 2024

Brand Name: Atlan Product Name: Atlan A300XL Model/Catalog Number: 8621400 The Atlan is an anesthesia workstation intended for use in anesthe…

FDA Devices Critical Nov 20, 2024

Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Component: Not applicable

FDA Devices Critical Nov 20, 2024

Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Component: Not applicable

FDA Devices Critical Aug 30, 2023

Carina Sub-Acute Care Ventilator

FDA Devices Critical Jul 19, 2023

Oxylog 3000 Plus emergency and transport ventilator

FDA Devices Critical May 24, 2023

VentStar Basic (P)180, MP00351

FDA Devices Critical May 24, 2023

Set2Go Ventilation 12 (A), MP07968

FDA Devices Critical May 24, 2023

Seattle PAP Plus, MP02260

FDA Devices Critical May 24, 2023

VentStar Anesthesia WT (P)180, MP00374

FDA Devices Critical May 24, 2023

Anesthesia Set Coax 180, MP03384

FDA Devices Critical May 24, 2023

VentStar Watertrap (N) 180, MP00363

FDA Devices Critical May 24, 2023

VentStar Watertrap (P) 180, MP00361

FDA Devices Critical May 24, 2023

VentStar Anesthesia (N) 180, MP00333

FDA Devices Critical May 24, 2023

Ventstar Coax, MP03373

FDA Devices Critical May 24, 2023

ID Circuit Basic (P) 180, MP01340

FDA Devices Critical May 24, 2023

VentStar Basic (P)250, MP00352

FDA Devices Critical May 24, 2023

Anesthesia Circuit Kit Coax 3, MP02732

FDA Devices Critical May 24, 2023

Ventstar Coax 180, MP03374

FDA Devices Critical May 24, 2023

Anesthesia Circuit Kit Coax 1, MP02730

FDA Devices Critical Mar 1, 2023

NovaStar TS, Standard elbow, Reusable, Material Numbers MP01579 (Size S), MP01580 (Size M), and MP01581 (Size L)

FDA Devices Critical Mar 1, 2023

NovaStar TS, Anti-Asphyxia Valve, Reusable, Material Numbers MP01576 (Size S), MP01577 (Size M), and MP01578 (Size L)

FDA Devices Critical Jun 22, 2022

Drager SafeStar 55, Catalog No. MP01790

FDA Devices Moderate Apr 13, 2022

Evita V500 Ventilator with Software 2.51.01 and Lower - intended for the ventilation of adult, pediatric and neonatal patients Catalog Number: 84164…

FDA Devices Moderate Apr 13, 2022

Babylog VN500 Ventilator with Software 2.51.01 and Lower- intended for the ventilation neonatal patients from 0.4 kg (0.88 lbs) up to 10 kg (22 lbs) …

FDA Devices Moderate Jan 26, 2022

Draeger Fabius MRI Anesthesia Machine, Catalog Number 8607300

FDA Devices Moderate Oct 20, 2021

Babylog VN500 Ventilator with Installed CO2 Measurement Option-intended for the ventilation of neonatal patients from 0.4 kg (0.88 lbs) up to 10 kg (…

FDA Devices Moderate Oct 20, 2021

Evita V500 Ventilator with Installed CO2 Measurement Option-Intended for the ventilation of adult,pediatric and neonatal patients. Catalog Number: 8…

FDA Devices Moderate Jun 9, 2021

Critical Care Ventilator, Catalog Number(s): 8422200: Babylog VN600 - Product Usage: used for treating patients who require temporary or longer term …

FDA Devices Moderate Jun 9, 2021

Critical Care Ventilator, Catalog Number(s): 8422300: Evita V600 - Product Usage: used for treating patients who require temporary or longer term res…

FDA Devices Moderate Jun 9, 2021

Critical Care Ventilator, Catalog Number(s): 8422500: Evita V800 - Product Usage: used for treating patients who require temporary or longer term res…

FDA Devices Moderate Jun 9, 2021

Critical Care Ventilator, Catalog Number(s): 8422400: Babylog VN800 - Product Usage: used for treating patients who require temporary or longer term …

FDA Devices Moderate Mar 17, 2021

ID Circuit Basic (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP01327 - Product Usage: Breathing circuit for conduction of respir…

FDA Devices Moderate Mar 17, 2021

VentStar Watertrap (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP00363 - Product Usage: Breathing circuit for conduction of respi…

FDA Devices Critical Jan 30, 2019

ID Circuit Basic 180, Catalog Number MP01350 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respira…

FDA Devices Critical Jan 30, 2019

VentStar Watertrap (P) 180, Catalog Number MP00361 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of r…

FDA Devices Critical Jan 30, 2019

VentStar Basic 250, Catalog Number MP00350 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respirator…

FDA Devices Critical Jan 30, 2019

ID Circuit Watertrap (P) 180, Catalog Number MP01341 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction o…

FDA Devices Critical Jan 30, 2019

VentStar Basic (P) 250, Catalog Number MP00352 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respi…

FDA Devices Critical Jan 30, 2019

VentStar Basic 180, Catalog Number MP00349 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respirato…

FDA Devices Critical Jan 30, 2019

VentStar Basic (P) 180, Catalog Number MP00351 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respi…

FDA Devices Critical Jan 30, 2019

ID Circuit Basic 250, Catalog Number MP01348 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respira…

FDA Devices Moderate Jun 27, 2018

Perseus A500 Anesthesia Machine; Cat. no. MK06000 Product V Product Usage: Intended for use in anesthetizing adults, children, and neonates an…

FDA Devices Moderate Jun 27, 2018

Fabius GS Tiro Anesthesia Machine; Cat. no. 8606000 Product Usage: Inhalation anesthesia machines for use in operating, induction and recovery ro…

FDA Devices Moderate Jun 27, 2018

Fabius GS Premium Anesthesia Machine; Cat. no. 8607000 Product Usage: Inhalation anesthesia machines for use in operating, induction and recovery…

FDA Devices Moderate Jun 27, 2018

Fabius GS MRI Anesthesia Machine; Cat. no. 8607300 Product Usage: Inhalation anesthesia machines for use in operating, induction and recovery roo…

FDA Devices Critical May 16, 2018

Fabius MRI, anesthesia machine, catalog no. 8607300 Product Usage: The products are inhalation anesthesia machines for use in operating, inductio…

FDA Devices Critical May 16, 2018

Fabius GS Premium, anesthesia machine, catalog no. 8607000 Product Usage: The products are inhalation anesthesia machines for use in operating, i…

FDA Devices Critical May 16, 2018

Fabius Tiro, anesthesia machine, catalog no. 8606000 Product Usage: The products are inhalation anesthesia machines for use in operating, inducti…

FDA Devices Critical Aug 10, 2016

Oxylog 3000, Disposable Pediatric Patient Circuit, Catalog Number: 5704964 The VentStar Oxylog 3000F disposable pediatric patient breathing circui…

FDA Devices Moderate Aug 3, 2016

Babytherm 8004/8010, Infant Warmer, Class II device, 510 K K971198, Catalog # FR00105 (Babytherm 8010), 2M30404 (Babytherm 8004), non sterile, softwa…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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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