The Recall Desk
SevereFDA (Devices)·Z-1446-2023·Announced 2023-05-24

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.

What this means for you

Illness, injury, or structural failure has been reported. 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.
Category
Medical Device — Respiratory Equipment
Hazard
  • loose-connection
  • detachment-risk

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.

Related recalls

Same category