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Locking Titanium Adapter for Peritoneal Dialysis Catheter

BAXTER INTERNATIONAL INC. · Model 5C4129 · UDI-DI 00085412007403

KDJ Prescription
10
510(k) clearances
72,474
Adverse events (2,405 deaths)
61
Recalls
22
Facilities

Description

This adapter is a double sealing female Luer lock adapter with a 2-piece, combination compression fit/barbed catheter connector. The adapter is used to connect the PD catheter to a solution transfer set with locking connector.

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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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.