Ventstar Coax 230, MP03376 — FDA record Z-1457-2023

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 17, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Ventstar Coax 230, MP03376
Reason
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Classification
Class I
Recalling firm
Draeger Medical, Inc.
Quantity
40 units
Agency-reported status
Terminated
Source record identifier
Z-1457-2023

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityUDI-DI: 04048675545613; All lots.

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

Domestic: US Nationwide Distribution.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
May 24, 2023
Recall initiation date
Apr 17, 2023
Center classification date
May 17, 2023
Termination date
Sep 3, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

Related records