Home › Fresenius Medical Care Holdings, Inc. › stay.safe®
stay.safe®
Fresenius Medical Care Holdings, Inc. · Model 050-95012 · UDI-DI 10840861100832
KDJ
Prescription
1
510(k) clearances
72,474
Adverse events (2,405 deaths)
61
Recalls
22
Facilities
Description
stay.safe® Cap
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. |
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 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.