ID Circuit Basic breathing circuit recalled for loose glued connections
Draeger Medical is recalling ID Circuit Basic breathing circuits due to glued connections that can loosen during ventilation, potentially causing partial or complete detachment of circuit pieces.
The agency’s classification
FDA (Devices): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: This is an FDA Class I medical device recall. The rubric requires that FDA Class I recalls score at least 4 (Severe). While no illnesses or injuries have been reported, the potential for partial or complete detachment of breathing circuit connections during ventilation poses a serious risk to patient respiratory support.
Plain-English summary
Draeger Medical, Inc. is recalling the ID Circuit Basic (P) 180, model MP01340 breathing circuits. The affected products have a nationwide distribution in the United States.
The breathing circuits have glued connections that can become loose before or during ventilation. This can result in partial or complete detachment of circuit pieces, potentially compromising the delivery of respiratory support.
All lots of the product are included in this recall. Healthcare facilities and users who have these breathing circuits should stop using them and contact Draeger Medical, Inc. for further guidance on replacement or remediation steps.
The recalled product
- Product
- ID Circuit Basic (P) 180, MP01340
- 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 (2)
- UDI-DI: 04048675421870
- All lots.
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 22 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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