FDA Device Intelligence
Home › Vantive US Healthcare LLC › MANIFOLD SET

MANIFOLD SET

Vantive US Healthcare LLC · Model L5C4446 · UDI-DI 07332414208417

KDJ Prescription
1
510(k) clearances
72,474
Adverse events (2,405 deaths)
61
Recalls
22
Facilities

Description

This set is designed for infusion of peritoneal dialysis solution. This set consists of a white luer lock connector (with blue pull ring cap) which is intended to connect to a supply line of an APD Set with Cassette and 5 blue luer lock connectors (with clear pull ring caps) which are intended to connect to solution bags (with Luers). Manifold Set 5-Prong

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.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data 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.