FDA Device Intelligence
HomeDevice types › KPE

Container, I.V.

FDA product code KPE · Class 2 · General Hospital

530
Registered devices
6,755
Adverse events
62
Recalls
117
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2024-10-09The Metrix CompanyA limited number of IV bags have been found to leak during filling.
2024-10-09The Metrix CompanyA limited number of IV bags have been found to leak during filling.
2024-10-09The Metrix CompanyA limited number of IV bags have been found to leak during filling.
2024-10-09The Metrix CompanyA limited number of IV bags have been found to leak during filling.
2024-10-09The Metrix CompanyA limited number of IV bags have been found to leak during filling.
2024-10-09The Metrix CompanyA limited number of IV bags have been found to leak during filling.
2024-10-09The Metrix CompanyA limited number of IV bags have been found to leak during filling.
2024-10-09The Metrix CompanyA limited number of IV bags have been found to leak during filling.
2024-10-09The Metrix CompanyA limited number of IV bags have been found to leak during filling.
2024-10-09The Metrix CompanyA limited number of IV bags have been found to leak during filling.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.