Medical Device Recalls
-
|
1 to 6 of 6 Results
510(K) Number: K101907 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| CS Elite Processing Set (125 ml) Autotransfusion Device - Product Usage:its related accessory compon... | 2 | 01/29/2020 |
FEI # 1219343 Haemonetics Corporation |
| CS Elite Processing Set (225 ml) Autotransfusion Device - Product Usage:its related accessory compon... | 2 | 01/29/2020 |
FEI # 1219343 Haemonetics Corporation |
| CS Elite Fastpack, 125 mL, 150 Res Autotransfusion Device - Product Usage: its related accessory com... | 2 | 01/29/2020 |
FEI # 1219343 Haemonetics Corporation |
| CS Elite Fastpack, 225 mL, 20® Res Autotransfusion Device - Product Usage: its related accessory com... | 2 | 01/29/2020 |
FEI # 1219343 Haemonetics Corporation |
| CS Elite Fastpack, 225 mL, 150 Res Autotransfusion Device - Product Usage: its related accessory com... | 2 | 01/29/2020 |
FEI # 1219343 Haemonetics Corporation |
| Cell Saver Elite Processing Kit, 70 ml, Product ID: CSE-P-70 Indications for Use: The Haemonetics... | 2 | 01/28/2019 |
FEI # 1219343 Haemonetics Corporation |
-







