PlainRecalls

Draeger, Inc.

Compiled from official public sources by the editorial team.

19 recalls on record · Latest: Dec 31, 2025

Draeger, Inc. Recall Insight

Draeger, Inc. appears on 19 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.019% 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 31, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 19 entries, severity tagging shows 19 critical, 0 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 19 of 19 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 (19). The date window on this page runs from Apr 9, 2025 to Dec 31, 2025.

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 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 pati…

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 patie…

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 …

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 pati…

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 an…

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 …

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: Breathin…

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 Pro…

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 P…

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 Pro…

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 Pro…

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 …

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: Brea…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Draeger, Inc. with Zimmer Biomet, Inc. →

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.