Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Recalled by Draeger, Inc. Due to The potential for cracks forming in the breathing...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Draeger, Inc. directly.
Affected Products
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 2 Model/Catalog Number: MP02738 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended for single use only Component: Not applicable
Quantity: 780 units
Why Was This Recalled?
The potential for cracks forming in the breathing circuit hose.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Draeger, Inc.
Draeger, Inc. has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report