PlainRecalls

Draeger Medical, Inc.

Compiled from official public sources by the publisher.

78 recalls on record · Latest: Dec 25, 2024

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Agency notice ledger

Federal filing book Draeger Medical, Inc. MID-BOOK · SINGLE-AGENCY

#232 of 14,151 · 78 notices · 0.075% archive

  • BOOK 78 notices
  • RANK #232 of 14,151
  • SHARE 0.075% archive
  • AGENCY FDA Devices (78)
  • CAT medical devices
  • CATS 1 category
  • LATEST Dec 25, 2024
  • PHOTO Angiodynamics Inc.

Nearest notice-volume peer: Angiodynamics Inc. (Navilyst Medical Inc.) (0 notice gap)

Draeger Medical, Inc. accounts for about 0.075% of the 104,423-notice archive on 78 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 Draeger Medical, Inc. sits among 14,151 recalling firms

Draeger Medical, Inc. ranks 232nd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Draeger Medical, Inc. vs all firms by recall-notice count

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

78 232nd of 14151 higher than 13,917 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

Draeger Medical, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Draeger Medical, Inc. holds about 0.075% of archive notices alongside 78 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
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 anesthetizing adults, pediatrics, and neonates.
FDA Devices Critical Dec 25, 2024

Brand Name: Atlan Product Name: Atlan A300 Model/Catalog Number: 8211300 The Atlan is an anesthesia workstation intended for use in anesthetizing adults, pediatrics, and neonates.
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 Apr 24, 2024

Dr¿ger Perseus A500 Anesthesia Workstation
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 May 24, 2023

VentStar Basic (N) 180, MP00353
FDA Devices Critical May 24, 2023

VentStar breathing bag Set (P) 110, MP00384
FDA Devices Critical May 24, 2023

Anesthesia Circuit Kit Coax HEPA, MP17102
FDA Devices Critical May 24, 2023

Ventstar Coax 230, MP03376
FDA Devices Critical May 24, 2023

VentStar Bag Set (N) 110, MP00383
FDA Devices Critical May 24, 2023

VentStar Watertrap (P) 180 w/oLL, MP00362
FDA Devices Critical May 24, 2023

VentStar Coax (P) 150, MP00379
FDA Devices Critical May 24, 2023

ID Coax 180, MP03375
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: 8416400
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) and pediatric patients from 5 kg (11 lbs) up to 20 kg (44 lbs) bodyweight Catalog Number: 8417400
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 (22 lbs) and pediatric patients from 5 kg (11 lbs) up to 20 kg (44 lbs) bodyweight. Catalog Number: 8417400
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: 8416400
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 respiratory support for different medical reasons.
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 respiratory support for different medical reasons.
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 respiratory support for different medical reasons.
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 respiratory support for different medical reasons.
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 respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.
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 respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.
FDA Devices Moderate Mar 17, 2021

VentStar Anesthesia (N) 180 - Drager Breathing Circuits/Anesthesia Sets Order Number: MP00333 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.
FDA Devices Moderate Mar 17, 2021

VentStar Basic (N) 180- Drager Breathing Circuits/Anesthesia Sets Order Number: MP00353 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.
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 respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water trap: Breathing circuit for conveying breathing gases between an anesthesia delivery system or ventilator and a pediatric patient. Intended for single use only. Water traps are intended for collection of conden
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 respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water trap: Breathing circuit for conveying breathing gases between an anesthesia delivery system or ventilator and a pediatric patient. Intended for single use only. Water traps are intended for collection of

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 respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water trap: Breathing circuit for conveying breathing gases between an anesthesia delivery system or ventilator and a pediatric patient. Intended for single use only. Water traps are intended for collection of condensat
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 of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water trap: Breathing circuit for conveying breathing gases between an anesthesia delivery system or ventilator and a pediatric patient. Intended for single use only. Water traps are intended for collection

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 respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water trap: Breathing circuit for conveying breathing gases between an anesthesia delivery system or ventilator and a pediatric patient. Intended for single use only. Water traps are intended for collection of cond

Draeger Medical, Inc. carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Frequently Asked Questions

How many federal recall notices name Draeger Medical, Inc.? ▼
PlainRecalls indexes 78 distinct federal recall events naming Draeger Medical, 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 Draeger Medical, Inc. sit among other recalling firms? ▼
Draeger Medical, Inc. ranks #232 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 Draeger Medical, Inc.'s notices? ▼
FDA Devices accounts for 78 of this firm's 78 indexed notices.
What product category dominates Draeger Medical, Inc.'s filing book? ▼
Filings for Draeger Medical, 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.
Draeger Medical, Inc.: 78 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 Draeger Medical, Inc.; individual notices remain authoritative on each linked recall page.

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