Medical Device Recalls
-
|
1 to 5 of 5 Results
510(K) Number: K173593 |
|
Results per Page |
|
Product Description
![Sort by Product Name [A-Z]](/scripts/cdrh/images/arrow_up-black.GIF){kind=icon} ![Sort by Product Name [Z-A]](/scripts/cdrh/images/arrow_down-black.GIF){kind=icon}
|
Recall
Class
|
FDA Recall
Posting Date
|
Recalling Firm
|
|---|---|---|---|
| stay-safe /Safe Lock Catheter Ext. 12 in | 1 | 03/26/2024 | Fresenius Medical Care Holdings, Inc. |
| stay-safe /Luer Lock Adapter 4 in | 1 | 03/26/2024 | Fresenius Medical Care Holdings, Inc. |
| stay-safe /Luer Catheter Ext. 6 in | 1 | 03/26/2024 | Fresenius Medical Care Holdings, Inc. |
| stay-safe /Luer Lock Catheter Ext. 18 in | 1 | 03/26/2024 | Fresenius Medical Care Holdings, Inc. |
| stay-safe /Luer Lock Catheter Ext. 12 in | 1 | 03/26/2024 | Fresenius Medical Care Holdings, Inc. |
-
