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Draeger Medical, Inc. recalls VentStar Watertrap (P) 180, Catalog Number MP00361 Breathing Circuits/Anesthesia Sets without a Water trap: Breathin
Recalled January 30, 2019 · FDA recall Z-0740-2019 · Draeger Medical
Hazard
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit · FDA Class I
Units
25 units
Sold at
US Distribution to states of: AL, CA, CO, CT, FL, KY, MI, NJ, OH, PA, SC & TX.
Description
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit
Product
VentStar Watertrap (P) 180, Catalog Number MP00361 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water trap: Breathing circuit for conveying breathing gases between an anesthesia delivery system or ventilator and a pediatric patient. Intended for single use only. Water traps are intended for collection of condensate. The standard breathing circuit is equipped with a water trap in each breathing hose limb.
Manufacturer(s)
Draeger Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →