Medical Device Recalls
-
1 to 4 of 4 Results
510(K) Number: K955644 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Synchron Systems Drug Calibrator 1 (Carbamaxepine, Phenobarbitol, Phentoin, Theophylline, and Valpro... | 2 | 07/20/2004 | Beckman Coulter Inc |
Synchron Phenobarbital (PHE) Drug Calibrator 1, P/N 469600, Classification Product Code: KLT. ... | 2 | 03/06/2012 | Beckman Coulter Inc. |
Synchron Phenobarbital (PHE) Reagent, P/N 469785, Classification Product Code: KLT. Subsequen... | 2 | 03/06/2012 | Beckman Coulter Inc. |
SYNCHRON Gentamicin (GEN) Reagent GEN reagent, when used in conjunction with SYNCHRON LX System(s),... | 2 | 09/20/2010 | Beckman Coulter Inc. |
-