PlainRecalls

Draeger, Inc.

Compiled from official public sources by the publisher.

21 recalls on record · Latest: Jun 10, 2026

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Agency notice ledger

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

#767 of 14,151 · 21 notices · 0.020% archive

  • BOOK 21 notices
  • RANK #767 of 14,151
  • SHARE 0.020% archive
  • AGENCY FDA Devices (21)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jun 10, 2026
  • PHOTO A&h Focal Inc.

Nearest notice-volume peer: A&h Focal Inc. (0 notice gap)

Draeger, Inc. accounts for about 0.020% of the 104,423-notice archive on 21 distinct filings — a mid 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, Inc. sits among 14,151 recalling firms

Draeger, Inc. ranks 767th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

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

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

21 767th of 14151 higher than 13,362 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, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Draeger, Inc. holds about 0.020% of archive notices alongside 21 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Critical Jun 10, 2026

Atlan A350XL. Model Number: 8621600. anesthesia workstation
FDA Devices Critical Jun 10, 2026

Atlan A350. Model Number: 8211500. anesthesia workstation
FDA Devices Critical Dec 31, 2025

Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer.
FDA Devices Critical Dec 31, 2025

Draeger Vapor 3000. Unheated, calibrated anesthetic vaporizer.
FDA Devices Critical Dec 17, 2025

ErgoStar CM 60, Model/Catalog Number: MP01860, Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a mechanically ventilated patient.
FDA Devices Critical Dec 17, 2025

ErgoStar CM 45, Model/Catalog Number: MP01845, Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a mechanically ventilated patient.
FDA Devices Critical Dec 17, 2025

ErgoStar CM 40 Model/Catalog Number: MP01840 Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a mechanically ventilated patient.
FDA Devices Critical Dec 17, 2025

ErgoStar CM 55, Model/Catalog Number: MP01855, Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a mechanically ventilated patient.
FDA Devices Critical Oct 8, 2025

Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Product Description: The Atlan is an anesthesia workstation intended for use in anesthetizing adults, pediatrics, and neonates. The device can be used for mechanical ventilation, manual ventilation, pressure-supported spontaneous breathing, and spontaneous breathing. The device is specified for inhalational anesthesia and/or patient ventilation in accordance with the intended use during

FDA Devices Critical Oct 8, 2025

Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Product Description: The Atlan is an anesthesia workstation intended for use in anesthetizing adults, pediatrics, and neonates. The device can be used for mechanical ventilation, manual ventilation, pressure-supported spontaneous breathing, and spontaneous breathing. The device is specified for inhalational anesthesia and/or patient ventilation in accordance with the intended use durin
FDA Devices Critical Aug 6, 2025

SafeStar 90 Plus Filter. Bidirectionally breathing system filter.
FDA Devices Critical Aug 6, 2025

SafeStar 55 Plus Filter. Bidirectionally breathing system filter.
FDA Devices Critical Aug 6, 2025

SafeStar 60A Plus Filter. Bidirectionally breathing system filter.
FDA Devices Critical Aug 6, 2025

HME TwinStar HEPA Plus Filter. Bidirectionally breathing system filter.
FDA Devices Critical Apr 9, 2025

Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number: MP00355 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult patients. The breathing circuit is intended for single use only. Component: Not applicable
FDA Devices Critical Apr 9, 2025

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 1 Model/Catalog Number: MP02737 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended for single use only Component: Not applicable
FDA Devices Critical Apr 9, 2025

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex EPA Model/Catalog Number: MP17103 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended for single use only
FDA Devices Critical Apr 9, 2025

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model/Catalog Number: MP02744 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended for single use only
FDA Devices Critical Apr 9, 2025

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 2 Model/Catalog Number: MP02738 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended for single use only Component: Not applicable
FDA Devices Critical Apr 9, 2025

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex (P)2 Model/Catalog Number: MP02752 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended for single use only Component: Not applicable
FDA Devices Critical Apr 9, 2025

Brand Name: ID Circuit Product Name: ID Circuit Flex 220 Model/Catalog Number: MP01347 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult Component: Not applicable

Draeger, Inc. holds a measurable archive slice

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 (21 here).

A&h Focal Inc. 21 Able Groupe Inc 21 Alvogen, Inc 21 Aroa Biosurgery, LTD. 21 Aston Martin 21

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Aroa Biosurgery, LTD. 21 Corin Ltd 21 Covidien 21 Custom Medical Specialties, Inc. 21

Frequently Asked Questions

How many federal recall notices name Draeger, Inc.? ▼
PlainRecalls indexes 21 distinct federal recall events naming Draeger, 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, Inc. sit among other recalling firms? ▼
Draeger, Inc. ranks #767 of 14,151 by distinct recall-event count among 14,151 firms in this archive (94th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Draeger, Inc.'s notices? ▼
FDA Devices accounts for 21 of this firm's 21 indexed notices.
What product category dominates Draeger, Inc.'s filing book? ▼
Filings for Draeger, 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, Inc.: 21 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, Inc.; individual notices remain authoritative on each linked recall page.

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