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Incident · Recall

FDA Class I recall of Dräger Oxylog emergency transport ventilators over ventilation halt risk

The FDA issued a Class I recall for 117 Dräger Oxylog 2000 plus, Oxylog 3000, and Oxylog 3000 plus emergency transport ventilators distributed across 39 states. An electrical issue could cause the ventilators to stop working if control knobs are not regularly used, potentially leading to insufficient oxygen delivery and patient injury or death.

Occurred 2016-01-07 · Dräger · Investigated by FDA

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Incident records on DEPLOY are compiled from public sources (regulatory filings, news reports, and operator disclosures) and reflect what has been reported and tracked to date. They are not legal findings, determinations of fault, or safety ratings, and may be updated as new information is verified. See the sources below for the underlying references.
Track FDA Class I recall of Dräger Oxylog emergency transport ventilators over ventilation halt risk

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Sources (1)

  1. MassDevice · https://www.massdevice.com/fda-drager-med-transport-ventilator-recall-is-class-i/ · 2016-01-07

Status history

  • Active · 2026-07-29 · agent:recon

Common questions

What happened in FDA Class I recall of Dräger Oxylog emergency transport ventilators over ventilation halt risk?
The FDA issued a Class I recall for 117 Dräger Oxylog 2000 plus, Oxylog 3000, and Oxylog 3000 plus emergency transport ventilators distributed across 39 states. An electrical issue could cause the ventilators to stop working if control knobs are not regularly used, potentially leading to insufficient oxygen delivery and patient injury or death.
When did this incident occur?
The incident is recorded as occurring on January 7, 2016 on the DEPLOY registry. The date reflects the underlying real-world event, not the registry record's creation date.
Who was involved in FDA Class I recall of Dräger Oxylog emergency transport ventilators over ventilation halt risk?
The incident is recorded as involving Dräger on the DEPLOY registry. No specific robot model is linked to this incident in the registry.
Has anyone responded to FDA Class I recall of Dräger Oxylog emergency transport ventilators over ventilation halt risk?
No responses to this incident are recorded on the DEPLOY registry. Operators, manufacturers, or affected parties can submit responses to the editorial team; absence is not a guarantee no response was issued.
What is the current status of FDA Class I recall of Dräger Oxylog emergency transport ventilators over ventilation halt risk?
This incident is an active record on the DEPLOY registry; no retraction or correction has been issued.
Methodology: Unreviewed · 1 source (no primary) · last reviewed 2026-07-29

Verification posture

Unreviewed

Low confidence

Review state

Stable

Last reviewed 2026-07-29

Sources by quality tier

1
unclassified
Unclassified source

The framework is documented at /methodology. Corrections at /corrections. Reviewer: DEPLOY editorial team.

Methodology surface for FDA Class I recall of Dräger Oxylog emergency transport ventilators over ventilation halt risk.

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Canonical ID 4374ca1f-6aea-455f-8d10-bdd74f9af072