Maquet Critical Care AB recalls 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…
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…
Read the official notice →- Date
- 2026-08-12
- Country
- United States
- Brand
- 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…
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution to the states of AL, AR, CA, CO, DC,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Maquet Critical Care AB recalls
- 2026-08-26
USMaquet Critical Care AB recalls GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuous ventilator system, for facility use.…
The module did not undergo electrical safety tests and functional tests during production.
FDA · DeviceMaquet Critical Care ABUS Nationwide distribution in the states of CA, GA, MN, NY.Official notice →- 2025-07-09
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Maquet Critical Care AB recalls Servo-u Ventilator System. Model Number: 6688600.
Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.
FDA · DeviceMaquet Critical Care ABUS Nationwide distribution and Puerto Rico. No international distribution.Official notice →
Other drugs & medical recalls in the United States
- 2026-08-12
- US
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Nuclein LLC recalls Brand Name: DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument Model/Catalog Number: SG-0002 Software Version: 6.0.2…
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Innovasis, Inc recalls Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System
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FDA · DeviceMedical Action Industries, Inc. 306US Nationwide distribution in the state of CA.Official notice → - US
Oxos Medical Inc recalls Brand Name: OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model/Catalog Number: MC2, MC2.1 Software Version: 5.7.0 Product…
Due to a defective circuit board that overheats
FDA · DeviceOxos Medical IncUS Nationwide distribution in the states of FL, GA, IN, SC, TX, VA.Official notice →