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Minicap
Vantive US Healthcare LLC · Model EZPC4466 · UDI-DI 07332414208264
KDJ
Prescription
1
510(k) clearances
72,474
Adverse events (2,405 deaths)
61
Recalls
22
Facilities
Description
This device is a plastic disconnect cap for peritoneal dialysis and contains povidone-iodine intended to protect the female Luer connector of the Baxter transfer set.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-10-23 | Baxter Healthcare Corporation | There 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. |
| 2024-10-23 | Baxter Healthcare Corporation | There 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. |
| 2024-10-23 | Baxter Healthcare Corporation | There 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. |
| 2024-10-23 | Baxter Healthcare Corporation | There 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. |
| 2024-10-23 | Baxter Healthcare Corporation | There 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. |
| 2024-10-23 | Baxter Healthcare Corporation | There 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. |
| 2024-10-23 | Baxter Healthcare Corporation | There 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. |
| 2024-10-23 | Baxter Healthcare Corporation | There 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. |
| 2024-10-23 | Baxter Healthcare Corporation | There 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. |
| 2024-10-23 | Baxter Healthcare Corporation | There 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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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.