Reported May 24, 2023 · Terminated
Ventstar Coax 230, MP03376
Draeger Medical, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Draeger Medical, Inc. · 3135 Quarry Rd · Telford, PA · 18969-1042
Is this the product you have?
Ventstar Coax 230MP03376
- Lot codes and dates
- UDI-DI04048675545613; All lots
- Amount recalled
- 40 units
This recall covers 22 products
The agency filed one notice per product. You are reading one of them; the other 21 are below.
9 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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