Drug recall
Life2000 Ventilator, Product Code: MS-01-0118, which is contained in the Life2000 Ventilator System, with…
FDA recall event 94701 · Class I · Baxter Healthcare Corporation
Key facts
| Event ID | 94701 |
|---|---|
| Recall numbers | Z-2140-2024 |
| Recalling firm | Baxter Healthcare Corporation |
| Product type | Devices |
| Products | Life2000 Ventilator, Product Code: MS-01-0118, which is contained in the Life2000 Ventilator System, with Product Codes BT-20-0002, BT-20-0002A and BT-20-0002AP. The Life2000 ventilation system… |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential for certain Life2000 ventilator systems to either fail to charge or have intermittent charging behavior due to damage to the battery charger dongle. Damage of the battery charger dongle… |
| Initiation date | May 29, 2024 |
| Report date | Jul 3, 2024 |
| City | Deerfield |
| State | IL |
| Country | United States |
| FEI number | 1417572 |
At a glance
- 1–9 Products in this recall
- 10–99 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: