Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Critical RiskFDA Device
Medical Devices

VentStar and Draeger Breathing Circuit Hoses Recalled for Potential Cracks

Agency Publication Date: April 3, 2025
Share:
Sign in to monitor this recall

Summary

Draeger, Inc. is recalling 388,925 breathing circuit hoses, including VentStar Flex and several Anesthesia Circuit Kits, because cracks may form in the hoses. These single-use circuits are used to deliver breathing gases between ventilators or anesthesia machines and adult patients. No injuries have been reported, but the cracks can lead to air leaks during medical procedures.

Risk

Cracks in the breathing circuit can cause a loss of breathing gas or pressure, which may result in a patient receiving inadequate ventilation or anesthesia during surgery or respiratory support.

What You Should Do

  1. This recall affects VentStar Flex 220, ID Circuit Flex 220, and several Anesthesia Circuit Kit Flex models (Flex 1, 2, 6, (P)2, and EPA) manufactured by Draeger, Inc.
  2. Check your inventory for model numbers MP00355, MP01347, MP02737, MP02738, MP02744, MP02752, and MP17103. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.
  4. Call the FDA at 1-888-463-6332 for more information regarding medical device recalls.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: VentStar Flex 220
Variants: Adult
Model / REF:
MP00355
Lot Numbers:
All lot numbers
UDI:
04048675248996

Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult patients.

Product: ID Circuit Flex 220
Variants: Adult
Model / REF:
MP01347
Lot Numbers:
All lot numbers
UDI:
04048675249337

Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult patients.

Product: Anesthesia Circuit Kit Flex 1
Variants: Single use
Model / REF:
MP02737
Lot Numbers:
All lot numbers
UDI:
04048675389620

Accessory for conducting medical gases between anesthesia machine and patient.

Product: Anesthesia Circuit Kit Flex 2
Variants: Single use
Model / REF:
MP02738
Lot Numbers:
All lot numbers
UDI:
04048675389637

Accessory for conducting medical gases between anesthesia machine and patient.

Product: Anesthesia Circuit Kit Flex 6
Variants: Single use
Model / REF:
MP02744
Lot Numbers:
All lot numbers
UDI:
040486775389675

Accessory for conducting medical gases between anesthesia machine and patient.

Product: Anesthesia Circuit Kit Flex (P)2
Variants: Single use
Model / REF:
MP02752
Lot Numbers:
All lot numbers
UDI:
04048675389729

Accessory for conducting medical gases between anesthesia machine and patient.

Product: Anesthesia Circuit Kit Flex EPA
Variants: Single use
Model / REF:
MP17103
Lot Numbers:
All lot numbers
UDI:
04048675695660

Accessory for conducting medical gases between anesthesia machine and patient.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96342
Status: Active
Manufacturer: Draeger, Inc.
Sold By: Medical device distributors; Direct hospital sales
Manufactured In: United States
Units Affected: 7 products (65150 units; 3325 units; 3140; 780 units; 293660 units; 9250 units; 13620 units)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.