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Devices and FDA recall records listed on MedWatcher for Maquet Critical Care AB.
This page covers the devices and recall records listed below, not the complete product catalogue or recall history. A recall may apply only to specific models, lots, or serial numbers.
Device and manufacturer names are linked using official product, UDI, or FDA records. The source links below show the supporting information.
Official records may use a legal name, brand, division, or shortened name. Similar names do not necessarily refer to the same manufacturer.
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.