Draeger ID Circuit Basic 180 Breathing Circuits Recalled for Assembly Defect
Draeger Medical is recalling 25 units of ID Circuit Basic 180 breathing circuits due to incorrect pre-assembly that may cause connection errors.
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 with a defect that poses a risk of harm (incorrect connection/short circuit) but the source text does not report any injuries or illnesses, fitting the 'High' severity criteria for risk-of-harm products where injury has not yet been reported.
Plain-English summary
Draeger Medical, Inc. is recalling 25 units of ID Circuit Basic 180 breathing circuits, Catalog Number MP01350. These single-use medical devices are intended to conduct respiratory gases between an anesthesia machine or ventilator and a patient. The recall covers all lots of the product.
The recall was initiated because the breathing circuits were incorrectly pre-assembled. This defect creates a potential for incorrect connection or a short circuit of the breathing circuit. The affected units were distributed in the United States to the states of Alabama, California, Colorado, Connecticut, Florida, Kentucky, Michigan, New Jersey, Ohio, Pennsylvania, South Carolina, and Texas.
Healthcare facilities and consumers who have these specific breathing circuits should stop using them immediately. Users should contact Draeger Medical, Inc. for further instructions on how to return or dispose of the affected units.
The recalled product
- Product
- ID Circuit Basic 180, Catalog Number MP01350 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets w
- 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
Part of a larger recall action
This product is one of 9 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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