FDA Device Intelligence
HomeDevice types › KDJ

Set, Administration, For Peritoneal Dialysis, Disposable

FDA product code KDJ · Class 2 · Gastroenterology, Urology

45
Registered devices
72,142
Adverse events
61
Recalls
113
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2024-10-23Baxter Healthcare CorporationThere has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
2024-10-23Baxter Healthcare CorporationThere has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
2024-10-23Baxter Healthcare CorporationThere has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
2024-10-23Baxter Healthcare CorporationThere has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
2024-10-23Baxter Healthcare CorporationThere has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
2024-10-23Baxter Healthcare CorporationThere has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
2024-10-23Baxter Healthcare CorporationThere has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
2024-10-23Baxter Healthcare CorporationThere has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
2024-10-23Baxter Healthcare CorporationThere has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
2024-10-23Baxter Healthcare CorporationThere has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

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