Life2000 Ventilator — Class I medical device recall Z-2140-2024
Ongoing recall by Baxter Healthcare Corporation, reported 2024-07-03, distributed nationwide. Potential for certain Life2000 ventilator systems to either fail to charge or have intermittent charging behav
| Recall number | Z-2140-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2024-05-29 |
| Classified | 2024-06-26 |
| Reported by FDA | 2024-07-03 |
| Distributed | Nationwide (US) |
| Quantity | 2,510 units |
| UPC / GTIN / UDI-DI | 00120210000758, 00120310000740, 00120310001433, 00120310001563, 00120310001631, 00120340001045, 00120350001042, 00120360000493, 00120360001001, 00120370001961, 00120380001616, 00120390000081, 00120390000784, 00120390001880, 00120400000025, 00120400000032, 00120400000049, 00120400001107, 00120400001145, 00120400001596, 00120420001286, 00120420001859, 00120430001368, 00120450000587, 00120450001331 and 196 more |
| Serial numbers | 120210000751, 120210000758, 120280000239, 120280000243, 120280000346, 120280000361, 120280000381, 120290000533, 120290000544, 120290000554, 120290000605, 120290000626, 120290000627, 120290000639, 120290000643, 120290001097, 120300000032, 120300000591, 120300000632, 120300000868, 120310000663, 120310000701, 120310000730, 120310000742, 120310001431 and 475 more |
Product
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 includes the Life2000 ventilator which has its individual label.
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 prevents the ventilator's internal battery from charging.
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-2140-2024. 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.