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Draeger Medical, Inc. recalls Carina Sub-Acute Care Ventilator
Recalled August 30, 2023 · FDA recall Z-2248-2023 · Draeger Medical
Hazard
Presence of polyether polyurethane (PE-PUR) and emission of 1,3-Dichloropropan-2-ol that exceed the acceptable uptake level during continuous use (>30 days) in pediatric patients. · FDA Class I
Units
11,621 units
Sold at
US Nationwide Distribution.
Description
Presence of polyether polyurethane (PE-PUR) and emission of 1,3-Dichloropropan-2-ol that exceed the acceptable uptake level during continuous use (>30 days) in pediatric patients.
Product
Carina Sub-Acute Care Ventilator
Manufacturer(s)
Draeger Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →