Dräger ID Circuit Basic Breathing Circuits Recalled for Detachment Risk
Dräger Medical is recalling ID Circuit Basic (N) 180 breathing circuits because the Y-piece may detach, causing a leak that hinders patient ventilation.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a medical device defect that can hinder patient ventilation, representing a risk of harm where injury has not yet been reported, which aligns with the 'High' severity criteria.
Plain-English summary
Dräger Medical, Inc. is recalling 25 units of ID Circuit Basic (N) 180-Drager Breathing Circuits/Anesthesia Sets (Order Number: MP01327). These products are intended for single use to conduct respiratory gases between an anesthesia machine or ventilator and a patient. The recall covers all lots and was distributed nationwide in the United States.
The recall was initiated because the Y-piece may become detached from the ventilation hose either before or during the ventilation process. This detachment can cause a leak that hinders the ventilation of the patient.
Healthcare facilities and users should stop using the affected breathing circuits immediately. They should contact Dräger Medical, Inc. for further instructions on how to return or dispose of the recalled units.
The recalled product
- Product
- 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.
- Manufacturer
- Draeger Medical, Inc.
- Affected units
- 25
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All lots
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 4 recalled by Draeger Medical, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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