VentStar Basic — Class I medical device recall Z-0739-2019
Terminated recall by Draeger Medical, Inc., reported 2019-01-30, distributed in AL, CA, CO, CT, FL, KY, MI, NJ…. Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breath
| Recall number | Z-0739-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Draeger Medical, Inc., Telford, PA, United States |
| Recall initiated | 2018-12-21 |
| Classified | 2019-01-24 |
| Reported by FDA | 2019-01-30 |
| Terminated | 2019-04-16 |
| Distributed | AL, CA, CO, CT, FL, KY, MI, NJ, OH, PA, SC, TX |
| Quantity | 75 units |
| Reason classes | device malfunction |
| Model numbers | MP00352 |
Product
VentStar Basic (P) 250, Catalog Number MP00352 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 for recall
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0739-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.