RecallRadar

FDA Device recall Z-0737-2019

VentStar Basic 250, Catalog Number MP00350 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of res…

On 2019-01-30 the FDA classified a Class I recall of VentStar Basic 250, Catalog Number MP00350 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of res… by Draeger Medical, citing incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0737-2019
ClassificationClass I
Statusterminated
Initiated2018-12-21
Published2019-01-30
Last updated2026-09-13 11:55 UTC
CompanyDraeger Medical
DistributionAL, CA, CO, CT, FL, KY, MI, NJ, OH, PA, SC, TX

Product

VentStar Basic 250, Catalog Number MP00350 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.

Reason

Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

Identifiers

code_infoAll Lots

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0737-2019%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.