Maquet Critical Care Ab: Gas-machine, Anesthesia
Recall Summary Maquet Critical Care AB is recalling multiple Flow anesthesia machines because the vaporizer may fail to deliver anesthetic agent when activated, potentially leaving patients under-anesthetized during surgery. This malfunction could result in patients waking up during procedures. The recall affects Flow-i and Flow-c/Flow-e models distributed nationwide across the United States.
- Recalling firm
- Maquet Critical Care AB
- Product
- Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530 Flow-i C40 6888540 Flow-c 6887700 Flow-e 6887900
- Reason
- Events observed where anesthetic agent was not delivered when the vaporizer was activated. Failure to deliver the anesthetic agent may result in the patient receiving insufficient anesthesia and may lead to intraoperative awareness.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-06-24
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Worldwide - US Nationwide distribution to the states of AL, AR, CA, CO, DC, DE, FL, GA, IN, MA, MI, MO, NY, OH, OR, PA, SC, TX, VA, WA, WV.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/4eeb2fdd-5181-402b-9e0d-754fcf0a8070