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INTRAVIA
BAXTER INTERNATIONAL INC. · Model 2B8012 · UDI-DI 00085412003191
KPE
Prescription
1
510(k) clearances
6,805
Adverse events (8 deaths)
62
Recalls
86
Facilities
Description
INTRAVIA Container, 250 mL Capacity
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
| 2024-10-09 | The Metrix Company | A limited number of IV bags have been found to leak during filling. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.