Reported Apr 9, 2025 · Ongoing
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex EPA Model/Catalog Number: MP17103 Software…
Draeger, 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, Inc. · 3135 Quarry Rd · Telford, PA · 18969-1042
Is this the product you have?
- Brand NameAnesthesia
- Circuit Kit Product NameAnesthesia Circuit
- Kit Flex EPA Model/Catalog NumberMP17103
- Software VersionNot
- applicable Product DescriptionAccessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended for single use only
- Lot codes and dates
- Model/Catalog Number
MP17103UDI Number 04048675695660All lot numbers
- Model/Catalog Number
- Amount recalled
- 13620 units
This recall covers 7 products
The agency filed one notice per product. You are reading one of them; the other 6 are below.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
The potential for cracks forming in the breathing circuit hose.
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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