Medical Device Recalls
-
1 to 4 of 4 Results
510(K) Number: K950958 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
SYNCHRON CX4 Delta Clinical System Part #: 468233 Product Usage: The Beckman SYNCHRON CX4 DELTA,... | 2 | 10/27/2011 | Beckman Coulter Inc. |
SYNCHRON CX9 Delta ALX System Part #: 473513 Product Usage: The Beckman SYNCHRON CX4 DELTA, CX7 ... | 2 | 10/27/2011 | Beckman Coulter Inc. |
SYNCHRON CX7 Delta Clinical System Part #: 468205 Product Usage: The Beckman SYNCHRON CX4 DELTA,... | 2 | 10/27/2011 | Beckman Coulter Inc. |
SYNCHRON CX5 Delta Clinical System Part #: 468243 Product Usage: The Beckman SYNCHRON CX4 DELTA,... | 2 | 10/27/2011 | Beckman Coulter Inc. |
-