Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0692-2016 — Emergency Transport Ventilator Oxylog 3000 Ventilator and Oxylog 3000 plus Ventilator Catalog Numbers: 2M86300/2M86965 and 5704813/5704831. Volume controlled and pressure-controlled emergency and transport ventilators.

U.S. FDA — Device Enforcement · United States · 2015-12-22 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0692-2016
Date of alert: 2015-12-22
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: Draeger Medical, Inc.
Product category: device
Product type: Devices

Reported risk: Drager became aware of situations where the error message "Poti unplugged" was generated causing acoustic and visual alarms, the breathing system releases pressure and the ventilation function stops operating.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-0692-2016 — Emergency Transport Ventilator Oxylog 3000 Ventilator and Oxylog 3000 plus Ventilator Catalog Numbers: 2M86300/2M86965 and 5704813/5704831. Volume controlled and pressure-controlled emergency and transport ventilators.

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