Draeger, Inc. recalls Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia
See all recalls from Draeger, Inc. →Recalled Product
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex EPA Model/Catalog Number: MP17103 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
Hazard / Issue
The potential for cracks forming in the breathing circuit hose.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Model/Catalog Number: MP17103; UDI Number 04048675695660; All lot numbers.
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Brand Name: Anesthesia Circuit →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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