Medical Device Recalls
-
|
1 to 3 of 3 Results
510(K) Number: K030209 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| MAHURKAR 13.5Fr High Flow Dual Lumen Acute Dialysis Catheter, Sterile, Single Use, Rx Only: 13.5... | 1 | 01/12/2023 |
FEI # 1282497 Covidien LP |
| Mahurkar QPlus Dual Lumen Catheter Kit with Curved Extension, 13.5 Fr/Ch x 19.5cm For hemodialysis... | 3 | 12/17/2003 |
FEI # 1282497 Kendall Healthcare Products Co |
| Mahurkar QPlus Dual Lumen Catheter Insertion Tray with Curved Extension, 13.5 Fr/Ch x 19.5cm For... | 3 | 12/17/2003 |
FEI # 1282497 Kendall Healthcare Products Co |
-







