Drug recall
ID Circuit Basic 180, Catalog Number MP01350 Breathing Circuits/Anesthesia Sets without a Water trap…
FDA recall event 81874 · Class I · Draeger Medical, Inc.
Key facts
| Event ID | 81874 |
|---|---|
| Recall numbers | Z-0736-2019, Z-0737-2019, Z-0738-2019, Z-0739-2019, Z-0740-2019, Z-0741-2019, Z-0742-2019, Z-0743-2019, Z-0744-2019 |
| Recalling firm | Draeger Medical, Inc. |
| Product type | Devices |
| Products | ID Circuit Basic 180, Catalog Number MP01350 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and…, ID Circuit Basic 250, Catalog Number MP01348 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and…, ID Circuit Watertrap (P) 180, Catalog Number MP01341 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or…, VentStar Anesthesia WT(P) 180, Catalog Number MP00374 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or…, VentStar Basic 180, Catalog Number MP00349 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and… and 4 more |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit |
| Initiation date | Dec 21, 2018 |
| Report date | Jan 30, 2019 |
| Termination date | Apr 16, 2019 |
| City | Telford |
| State | PA |
| Country | United States |
| FEI number | 2517967 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: